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MedTech Europe

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Namestring
MedTech Europe
Legal namestring
MedTech Europe AISBL
Company typeenum
Private
Founded yearint
2012
Descriptiontext

MedTech Europe is the European trade association for the medical technology industry, legally constituted as MedTech Europe AISBL, a non-profit international association under Belgian law headquartered in Brussels. Founded in October 2012 through the alliance of EDMA (the former European In Vitro Diagnostics association) and Eucomed (the former European Medical Devices association), the organization represents manufacturers of medical devices, in vitro diagnostics, and digital health solutions operating in Europe. Its membership comprises more than 140 multinational corporations — including Abbott, Roche, Siemens Healthineers, Medtronic, Philips, Stryker, Johnson & Johnson, Boston Scientific, Terumo, Zimmer Biomet, bioMérieux, Hologic, Alcon, Beckman Coulter, and Illumina — alongside more than 45 national medical technology trade associations that collectively represent approximately 38,000 companies across Europe, 90% of which are SMEs.

The association's core product portfolio is built around policy advocacy, regulatory guidance, market intelligence, and industry convening rather than proprietary technology. Functional offerings include the flagship MedTech Forum annual conference (Stockholm, May 11–13, 2026), the MedTech Monthly newsletter, the MedTech Views content platform, the Data Hub market intelligence service, the Conference Vetting System (CVS) for ethical compliance, sector groups covering Cardiovascular, Diabetes, Cancer, Wound Care, Orthopaedic, AMR/HAI and Robotic-Assisted Surgery, and the MedTech Europe Resource Library of position papers and regulatory guidance. The organization also manages industry participation in the Innovative Health Initiative (IHI), the EU public-private research partnership under Horizon Europe (2021–2027).

MedTech Europe is funded through recurring membership dues from corporate members, national association members, and supporter organizations, structured by company type and size (specific pricing is not publicly disclosed). Revenue is supplemented by event sponsorships, publication licensing, and partner-funded programs. The association is governed by a Board of Directors chaired by Stuart Silk (President EMEA, Latin America and Canada at Stryker), with day-to-day operations led by CEO Oliver Bisazza (appointed January 2023) and a secretariat of approximately 45–55 staff based in Brussels. The association does not pursue external funding rounds, has no parent company or subsidiaries, and operates without equity capital.

Short descriptiontext

MedTech Europe is the Brussels-based European trade association representing the medical technology industry — including medical devices, in vitro diagnostics, and digital health — through policy advocacy, regulatory guidance on MDR/IVDR, market data, and events. It serves 140+ multinational manufacturers and 45+ national associations covering ~38,000 European medtech companies.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBrussels, Belgium
HQ citystring
Brussels
HQ countrystring
Belgium
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
medical technology industry, regulatory advocacy services, trade association services, healthcare market data, medical device policy
Industry1 code
1Health, Pharmaceuticals & Medical Devices Regulatory Cooperation
CodeBPADANAJPrimaryYes
Product category
Medical Technology Industry Trade Association
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model1 record
1Membership Fees
TypeSubscription Recurring
Description

MedTech Europe generates revenue through membership fees from corporate members (medical technology manufacturers), associate corporate members, national association members, and supporter organizations. The association represents over 140 multinational corporations and more than 45 medical technology associations.

medtecheurope.org
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Operations, Marketing or Sales, Technology or R&D, Others
GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 4 records shown
1MedTech Forum
Description

Annual conference organized by MedTech Europe bringing together industry leaders to discuss innovation and regulation in Europe's medical device and IVD sector.

medtecheurope.org
+3 more records
Core offering1 text field

MedTech Europe is the European trade association representing the medical technology industry, including diagnostics, medical devices, and digital health. It provides policy advocacy, regulatory guidance on MDR/IVDR, market data services, international affairs representation, research and innovation facilitation (including the Innovative Health Initiative), sector-specific working groups, an annual flagship conference (The MedTech Forum), and ethical compliance services such as the Conference Vetting System (CVS).

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • The MedTech Forum 2026 brought together industry leaders in Stockholm to discuss innovation and regulation, showcasing the association's role in convening the sector.
+2 more records
Product overview1 text field

MedTech Europe is a European trade association representing the medical technology industries, from diagnosis to cure. Rather than offering a single unified product, the organization provides a portfolio of services including the MedTech Monthly newsletter, The MedTech Forum annual conference, the MedTech Views content platform, a Data Hub for market intelligence, and various sector groups covering Cardiovascular, Diabetes, Cancer, Wound Care, Orthopaedic, and AMR/HAIS. The association also manages the Conference Vetting System for ethical compliance, participates in the Innovative Health Initiative (IHI) partnership, and maintains a Resource Library of policy documents and guidance. These offerings collectively support advocacy, networking, market intelligence, and regulatory engagement for member companies operating in Europe's medical technology sector.

Product and service3 records
1The MedTech Forum
CategoryConference / Event
Description

The MedTech Forum is the flagship annual conference of MedTech Europe, bringing together industry leaders, policymakers, and stakeholders to discuss innovation and regulation in Europe's medical device and in vitro diagnostics sector. It is a paid event that attendees register for as a standalone offering.

2MedTech Europe Data Hub
CategoryMarket Data / Analytics Service
Description

The Data Hub provides market data services including flagship trackers that analyze market size, trends, and industry dynamics across the European medical technology sector, supporting evidence-based insights for member companies.

3Conference Vetting System (CVS)
CategoryCompliance Service
Description

The Conference Vetting System (CVS) is a compliance service operated via EthicalMedTech that assesses Third Party Educational Events to ensure ethical business practices in interactions with Healthcare Professionals and Organizations.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership7 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-14
Description

Mecomed, the Medical Technology Association in the Middle East and Africa, and MedTech Europe co-hosted a joint event at WHX Dubai 2026. Discussions focused on MDR and IVDR revisions' impact on the Middle East and Africa region, artificial intelligence regulations, and how global-regional collaboration can accelerate innovation and expand patient access to advanced medical technologies. The partnership aims to promote greater policy alignment, share best practices, and support policies that enable safe, responsible innovation across the MedTech ecosystem.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-05-14
Description

CEPS organized an in-person conference titled 'AI in health: shaping the future' in collaboration with PwC, bringing together EU policy makers, industry leaders, and researchers to discuss Europe's progress in deploying AI across diagnostics, personalized medicine, and hospital optimization. MedTech Europe participated with representatives featured in panel discussions alongside Sanofi and various research institutions.

Strategic tierMinorTypeImplementation/ SI/ Consulting Partner
Description

PwC co-organized the CEPS conference 'AI in health: shaping the future' focused on AI deployment in healthcare diagnostics, personalized medicine, and hospital optimization, addressing legislative frameworks including EU AI Act, European Health Data Space Regulation, and European Biotech and Biomanufacturing Act.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Mölnlycke, a global MedTech company headquartered in Sweden, welcomed the publication of a joint industry white paper by MedTech Europe's Wound Care Sector Working Group on the chronic wound crisis in Europe. The white paper reports that up to 14.9 million Europeans suffer from chronic wounds, consuming up to 4% of European healthcare budgets.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

The Innovative Health Initiative (IHI) is a public-private partnership between the European Union and European life science industries, under the EU R&I funding programme Horizon Europe. IHI was launched in 2021 and will run until 2027. MedTech Europe facilitates member participation in IHI projects and research collaborations.

Strategic tierCoreTypeOthers
Description

MedTech Europe engages extensively with the European Commission on regulatory policy, including MDR/IVDR revision discussions, Digital Health initiatives, and EU healthcare strategy. The association provides feedback on proposed regulations and advocates for innovation-friendly frameworks.

Strategic tierMinorTypeGTM or Marketing Partner
Description

BBC StoryWorks Commercial Productions produced the 'Connecting the Dots' video series for MedTech Europe, highlighting pioneering medical devices, diagnostic solutions, and services improving patient outcomes. The series won industry awards.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

The leading US medical technology industry association representing medical device, diagnostic, and digital health manufacturers. Directly comparable to MedTech Europe in scope and mission — serving as the US counterpart in transatlantic advocacy and offering a benchmark for dues-funded trade association economics in the medtech sector.

TypeDirect peer
Description

The Asia Pacific medical technology trade association, with similar advocacy and member-services scope covering medical devices, IVD, and digital health across APAC. Highly comparable in role as regional trade body, and a natural partner/counterpart of MedTech Europe in global regulatory alignment initiatives.

TypeDirect peer
Description

The Medical Technology Association serving the Middle East and Africa. Directly comparable as a regional medical devices/IVD trade body; already a strategic partner of MedTech Europe (joint events at WHX Dubai 2026), illustrating geographic complementarity.

TypeDirect peer
Description

The European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry. Comparable as a European-level trade association within the broader medtech ecosystem, focusing on medical imaging and digital health — overlapping with MedTech Europe's digital health and IVD/diagnostic dossiers.

5ABHI
TypeRegional player
Description

The UK HealthTech association serving as the leading national trade body for medical technology companies in the United Kingdom. Comparable as a national member association of MedTech Europe; CEO Peter Ellingworth sits on MedTech Europe's Board and on the MHRA's AI in Healthcare Commission.

TypeRegional player
Description

The German Medical Technology Association representing over 200 medtech companies in Germany, with deep policy and regulatory engagement in Berlin. Comparable as a national MedTech Europe member association and Board seat (MD Marc-Pierre Möll), the largest European medtech market.

TypeRegional player
Description

The Spanish Federation of Healthcare Technology Companies, the leading national MedTech trade association in Spain. Comparable as a national MedTech Europe member association with Board representation, addressing MDR/IVDR and market-access issues at the Spanish level.

TypeRegional player
Description

The French Medical Devices Industry Trade Association (Syndicat National de l'Industrie des Technologies Médicales). Comparable as a national MedTech Europe member association working on EU regulatory implementation and French market access for medical devices and IVD.

TypeRegional player
Description

Verband der Diagnostica-Industrie, the German IVD industry association with 100 member companies. Comparable as a MedTech Europe Board member association focused on the IVD/regulatory dossier, representing the largest European IVD market.

TypeRegional player
Description

The Polish Chamber of Commerce of Medical Devices, representing Polish medtech manufacturers. Comparable as a national MedTech Europe member association with Board representation, and active on EU MDR/IVDR alignment in Central and Eastern Europe.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

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Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers10 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

Integration4 records

Each record includes

Title, Type, Description, Source

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles11 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

MedTech Europe

Medical Technology Industry Trade Associationmedtecheurope.org

MedTech Europe is the Brussels-based European trade association representing the medical technology industry — including medical devices, in vitro diagnostics, and digital health — through policy advocacy, regulatory guidance on MDR/IVDR, market data, and events. It serves 140+ multinational manufacturers and 45+ national associations covering ~38,000 European medtech companies.

What MedTech Europe does

MedTech Europe is the European trade association for the medical technology industry, legally constituted as MedTech Europe AISBL, a non-profit international association under Belgian law headquartered in Brussels. Founded in October 2012 through the alliance of EDMA (the former European In Vitro Diagnostics association) and Eucomed (the former European Medical Devices association), the organization represents manufacturers of medical devices, in vitro diagnostics, and digital health solutions operating in Europe. Its membership comprises more than 140 multinational corporations — including Abbott, Roche, Siemens Healthineers, Medtronic, Philips, Stryker, Johnson & Johnson, Boston Scientific, Terumo, Zimmer Biomet, bioMérieux, Hologic, Alcon, Beckman Coulter, and Illumina — alongside more than 45 national medical technology trade associations that collectively represent approximately 38,000 companies across Europe, 90% of which are SMEs.

The association's core product portfolio is built around policy advocacy, regulatory guidance, market intelligence, and industry convening rather than proprietary technology. Functional offerings include the flagship MedTech Forum annual conference (Stockholm, May 11–13, 2026), the MedTech Monthly newsletter, the MedTech Views content platform, the Data Hub market intelligence service, the Conference Vetting System (CVS) for ethical compliance, sector groups covering Cardiovascular, Diabetes, Cancer, Wound Care, Orthopaedic, AMR/HAI and Robotic-Assisted Surgery, and the MedTech Europe Resource Library of position papers and regulatory guidance. The organization also manages industry participation in the Innovative Health Initiative (IHI), the EU public-private research partnership under Horizon Europe (2021–2027).

MedTech Europe is funded through recurring membership dues from corporate members, national association members, and supporter organizations, structured by company type and size (specific pricing is not publicly disclosed). Revenue is supplemented by event sponsorships, publication licensing, and partner-funded programs. The association is governed by a Board of Directors chaired by Stuart Silk (President EMEA, Latin America and Canada at Stryker), with day-to-day operations led by CEO Oliver Bisazza (appointed January 2023) and a secretariat of approximately 45–55 staff based in Brussels. The association does not pursue external funding rounds, has no parent company or subsidiaries, and operates without equity capital.

MedTech Europe firmographics

Firmographics
Name
MedTech Europe
Legal name
MedTech Europe AISBL
Website
https://medtecheurope.org
Company type
Private
Founded year
2012
Operating status
Operating
Headcount range
11–50 employees
Short description
MedTech Europe is the Brussels-based European trade association representing the medical technology industry — including medical devices, in vitro diagnostics, and digital health — through policy advocacy, regulatory guidance on MDR/IVDR, market data, and events. It serves 140+ multinational manufacturers and 45+ national associations covering ~38,000 European medtech companies.
Ownership category
akta.pro rank

MedTech Europe industry classification

Industry
Product category
Medical Technology Industry Trade Association
akta.pro primary industry
Health, Pharmaceuticals & Medical Devices Regulatory Cooperation (BPADANAJ)

Keywords

  • Medical technology industry
  • Regulatory advocacy services
  • Trade association services
  • Healthcare market data
  • Medical device policy

Where MedTech Europe is headquartered

Location

Headquarters

HQ city
Brussels
HQ country
Belgium
HQ region
Europe

Offices1 record

Markets served

MedTech Europe business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Marketing or Sales, Technology or R&D, Others

Revenue model

  1. Membership Fees: MedTech Europe generates revenue through membership fees from corporate members (medical technology manufacturers), associate corporate members, national association members, and supporter organizations. The association represents over 140 multinational corporations and more than 45 medical technology associations.

Go-to-market motion2 records

Distribution channels3 records

Marketing channels8 records

MedTech Europe product offering

Product offering

Core offering

MedTech Europe is the European trade association representing the medical technology industry, including diagnostics, medical devices, and digital health. It provides policy advocacy, regulatory guidance on MDR/IVDR, market data services, international affairs representation, research and innovation facilitation (including the Innovative Health Initiative), sector-specific working groups, an annual flagship conference (The MedTech Forum), and ethical compliance services such as the Conference Vetting System (CVS).

Product overview

MedTech Europe is a European trade association representing the medical technology industries, from diagnosis to cure. Rather than offering a single unified product, the organization provides a portfolio of services including the MedTech Monthly newsletter, The MedTech Forum annual conference, the MedTech Views content platform, a Data Hub for market intelligence, and various sector groups covering Cardiovascular, Diabetes, Cancer, Wound Care, Orthopaedic, and AMR/HAIS. The association also manages the Conference Vetting System for ethical compliance, participates in the Innovative Health Initiative (IHI) partnership, and maintains a Resource Library of policy documents and guidance. These offerings collectively support advocacy, networking, market intelligence, and regulatory engagement for member companies operating in Europe's medical technology sector.

Differentiator

Problem solved

Functional benefit

Brands

  • MedTech Forum: Annual conference organized by MedTech Europe bringing together industry leaders to discuss innovation and regulation in Europe's medical device and IVD sector.
  • MedTech Views
  • #PowerOfMedtech
  • Connecting the Dots

Products and services

  • The MedTech Forum The MedTech Forum is the flagship annual conference of MedTech Europe, bringing together industry leaders, policymakers, and stakeholders to discuss innovation and regulation in Europe's medical device and in vitro diagnostics sector. It is a paid event that attendees register for as a standalone offering.
  • MedTech Europe Data Hub The Data Hub provides market data services including flagship trackers that analyze market size, trends, and industry dynamics across the European medical technology sector, supporting evidence-based insights for member companies.
  • Conference Vetting System (CVS) The Conference Vetting System (CVS) is a compliance service operated via EthicalMedTech that assesses Third Party Educational Events to ensure ethical business practices in interactions with Healthcare Professionals and Organizations.

Quantifiable outcome

  • The MedTech Forum 2026 brought together industry leaders in Stockholm to discuss innovation and regulation, showcasing the association's role in convening the sector.
  • +2 more outcomes

Companies that use MedTech Europe

Customer profile

Named customers10 records

Segments4 records

Ideal customer profiles3 records

MedTech Europe technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Integration4 records

MedTech Europe partnerships and signals

Strategic signal

Partnerships

Seven partnerships are on record, tiered core and minor.

  • MecomedcoreStrategic or Co-development Partner · 14 February 2026Mecomed, the Medical Technology Association in the Middle East and Africa, and MedTech Europe co-hosted a joint event at WHX Dubai 2026. Discussions focused on MDR and IVDR revisions' impact on the Middle East and Africa region, artificial intelligence regulations, and how global-regional collaboration can accelerate innovation and expand patient access to advanced medical technologies. The partnership aims to promote greater policy alignment, share best practices, and support policies that enable safe, responsible innovation across the MedTech ecosystem.
  • CEPS (Centre for European Policy Studies)coreStrategic or Co-development Partner · 14 May 2025CEPS organized an in-person conference titled 'AI in health: shaping the future' in collaboration with PwC, bringing together EU policy makers, industry leaders, and researchers to discuss Europe's progress in deploying AI across diagnostics, personalized medicine, and hospital optimization. MedTech Europe participated with representatives featured in panel discussions alongside Sanofi and various research institutions.
  • PwCminorImplementation/ SI/ Consulting PartnerPwC co-organized the CEPS conference 'AI in health: shaping the future' focused on AI deployment in healthcare diagnostics, personalized medicine, and hospital optimization, addressing legislative frameworks including EU AI Act, European Health Data Space Regulation, and European Biotech and Biomanufacturing Act.
  • MölnlyckecoreStrategic or Co-development PartnerMölnlycke, a global MedTech company headquartered in Sweden, welcomed the publication of a joint industry white paper by MedTech Europe's Wound Care Sector Working Group on the chronic wound crisis in Europe. The white paper reports that up to 14.9 million Europeans suffer from chronic wounds, consuming up to 4% of European healthcare budgets.
  • Innovative Health Initiative (IHI)coreStrategic or Co-development PartnerThe Innovative Health Initiative (IHI) is a public-private partnership between the European Union and European life science industries, under the EU R&I funding programme Horizon Europe. IHI was launched in 2021 and will run until 2027. MedTech Europe facilitates member participation in IHI projects and research collaborations.
  • European CommissioncoreOthersMedTech Europe engages extensively with the European Commission on regulatory policy, including MDR/IVDR revision discussions, Digital Health initiatives, and EU healthcare strategy. The association provides feedback on proposed regulations and advocates for innovation-friendly frameworks.
  • BBC StoryWorks Commercial ProductionsminorGTM or Marketing PartnerBBC StoryWorks Commercial Productions produced the 'Connecting the Dots' video series for MedTech Europe, highlighting pioneering medical devices, diagnostic solutions, and services improving patient outcomes. The series won industry awards.

Scale indicators7 records

Recent moves7 records

Expansion highlights6 records

MedTech Europe competitors and assessment

Company assessment

Direct peers

  • AdvaMed: The leading US medical technology industry association representing medical device, diagnostic, and digital health manufacturers. Directly comparable to MedTech Europe in scope and mission — serving as the US counterpart in transatlantic advocacy and offering a benchmark for dues-funded trade association economics in the medtech sector.
  • APACMed: The Asia Pacific medical technology trade association, with similar advocacy and member-services scope covering medical devices, IVD, and digital health across APAC. Highly comparable in role as regional trade body, and a natural partner/counterpart of MedTech Europe in global regulatory alignment initiatives.
  • Mecomed: The Medical Technology Association serving the Middle East and Africa. Directly comparable as a regional medical devices/IVD trade body; already a strategic partner of MedTech Europe (joint events at WHX Dubai 2026), illustrating geographic complementarity.
  • COCIR: The European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry. Comparable as a European-level trade association within the broader medtech ecosystem, focusing on medical imaging and digital health — overlapping with MedTech Europe's digital health and IVD/diagnostic dossiers.

Regional players

  • ABHI: The UK HealthTech association serving as the leading national trade body for medical technology companies in the United Kingdom. Comparable as a national member association of MedTech Europe; CEO Peter Ellingworth sits on MedTech Europe's Board and on the MHRA's AI in Healthcare Commission.
  • BVMed: The German Medical Technology Association representing over 200 medtech companies in Germany, with deep policy and regulatory engagement in Berlin. Comparable as a national MedTech Europe member association and Board seat (MD Marc-Pierre Möll), the largest European medtech market.
  • FENIN: The Spanish Federation of Healthcare Technology Companies, the leading national MedTech trade association in Spain. Comparable as a national MedTech Europe member association with Board representation, addressing MDR/IVDR and market-access issues at the Spanish level.
  • SNITEM: The French Medical Devices Industry Trade Association (Syndicat National de l'Industrie des Technologies Médicales). Comparable as a national MedTech Europe member association working on EU regulatory implementation and French market access for medical devices and IVD.
  • VDGH: Verband der Diagnostica-Industrie, the German IVD industry association with 100 member companies. Comparable as a MedTech Europe Board member association focused on the IVD/regulatory dossier, representing the largest European IVD market.
  • POLMED: The Polish Chamber of Commerce of Medical Devices, representing Polish medtech manufacturers. Comparable as a national MedTech Europe member association with Board representation, and active on EU MDR/IVDR alignment in Central and Eastern Europe.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

MedTech Europe social profiles

Digital presence

MedTech Europe financial estimates

Financial estimate

Revenue estimate

Valuation estimate

MedTech Europe leadership team

Management profile

Number of profiles

Profiles11 records

MedTech Europe funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

MedTech Europe M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about MedTech Europe

What does MedTech Europe do?

MedTech Europe is the European trade association representing the medical technology industry, including diagnostics, medical devices, and digital health. It provides policy advocacy, regulatory guidance on MDR/IVDR, market data services, international affairs representation, research and innovation facilitation (including the Innovative Health Initiative), sector-specific working groups, an annual flagship conference (The MedTech Forum), and ethical compliance services such as the Conference Vetting System (CVS).

Is MedTech Europe a public or private company?

MedTech Europe is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was MedTech Europe founded?

MedTech Europe was founded in 2012. It employs 11 to 50 people.

Where is MedTech Europe based?

MedTech Europe is headquartered in Brussels, Belgium, in the Europe region.

How does MedTech Europe make money?

One revenue line is on record: membership Fees.

Who are MedTech Europe's main competitors?

Direct peers on record are AdvaMed, APACMed, Mecomed and COCIR. Regional players are ABHI, BVMed, FENIN, SNITEM, VDGH and POLMED.

Does MedTech Europe have an API?

No public API is recorded for MedTech Europe.

What industry is MedTech Europe in?

MedTech Europe's product category is Medical Technology Industry Trade Association. Its primary akta.pro industry code is BPADANAJ, Health, Pharmaceuticals & Medical Devices Regulatory Cooperation.

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Live signals
Medical Device NetworkThe 2026 MedTech Forum: innovation and regulation lead the agendaThe MedTech Forum convened in Stockholm, Sweden from May 11-13, 2026, bringing together industry leaders to discuss innovation and regulation in Europe's medical device and in vitro diagnostics sector. The European Medicines Agency (EMA) showcased its newly launched innovative device pathway pilot, a voluntary regulatory program aimed at accelerating patient access to novel medical technologies, with Class III and implantable devices as initial target categories. The conference also highlighted ongoing concerns about the EU's In Vitro Diagnostic Regulation (IVDR), with industry representatives warning that about a third of larger companies now prioritize launching products outside Europe first, prompting calls from MedTech Europe for regulatory rebalancing to make the framework more innovation-friendly.RapsEuro Roundup: MedTech Europe seeks changes to proposed MDR revisionsMedTech Europe has provided feedback on proposed revisions to the European Union’s medical device and diagnostic regulations, supporting some changes while proposing modifications to others. The trade group emphasizes the need for regulatory reforms to prevent delays, reduce costs, and improve innovation and patient access within the EU.CEPSAI in health: shaping the future – CEPSCEPS has announced an in-person conference titled 'AI in health: shaping the future' to be held in Brussels on May 14, 2025, bringing together EU policy makers, industry leaders, and researchers to discuss Europe's progress in deploying AI across diagnostics, personalized medicine, and hospital optimization. The event, organized in collaboration with PwC, will address key legislative frameworks including the EU AI Act, European Health Data Space Regulation, and European Biotech and Biomanufacturing Act, while acknowledging persistent challenges such as data fragmentation, uneven system readiness, and uncertainty around operationalizing new regulatory obligations. The conference will feature keynotes from European Commission officials and panel discussions with representatives from MedTech Europe, Sanofi, and various research institutions, setting the stage for the What's Next | Healthcare Series 2026.PR NewswireEurope faces a growing chronic wound crisis - time to act is nowMölnlycke, a global MedTech company, welcomed the publication of the white paper "Shaping the future of wound care in Europe" by the MedTech Europe Wound Care Sector Working Group, highlighting that up to 14.9 million people in Europe suffer from chronic wounds consuming up to 4% of European healthcare budgets. The white paper identifies three priority areas for reform and outlines four recommendations urging EU policymakers to elevate wound care as a strategic health priority. Mölnlycke emphasized that value-based healthcare represents the most sustainable path to improving prevention, earlier diagnosis, and patient outcomes across European health systems.PR NewswireEurope faces a growing chronic wound crisis - time to act is nowMölnlycke welcomes the publication of a joint industry white paper from MedTech Europe highlighting that up to 14.9 million Europeans suffer from chronic wounds, consuming up to 4% of European healthcare budgets. The white paper identifies three priority areas for reform and four recommendations for coordinated action among policymakers, clinicians, payers, patient organisations, and industry to address chronic wound care. The company emphasizes that chronic wounds are preventable and calls for EU policymakers to prioritize prevention, strengthen clinician training, and build integrated care pathways.news.cision.comEurope faces a growing chronic wound crisis – time to act is nowMölnlycke, a global MedTech company headquartered in Sweden, welcomed the publication of a joint industry white paper by MedTech Europe’s Wound Care Sector Working Group on the growing chronic wound crisis in Europe. The white paper reports that up to 14.9 million Europeans suffer from chronic wounds, consuming up to 4% of European healthcare budgets, with conditions like diabetic foot ulcers carrying a five-year mortality rate comparable to certain cancers. The paper urges EU policymakers to prioritize wound care as a strategic health priority, outlining four recommendations for coordinated action among policymakers, clinicians, payers, patient organisations, and industry.LogisticsGulfMecomed and MedTech Europe unite at WHX Dubai 2026Mecomed and MedTech Europe co-hosted a joint event at WHX Dubai 2026, bringing together MedTech leaders, policymakers, and industry stakeholders from around the world. The discussions focused on MDR and IVDR revisions' impact on the Middle East and Africa region, artificial intelligence regulations, and how global-regional collaboration can accelerate innovation and expand patient access to advanced medical technologies. The partnership aims to promote greater policy alignment, share best practices, and support policies that enable safe, responsible innovation across the MedTech ecosystem.ZawyaMecomed and MedTech Europe unite at WHX Dubai to advance medtech collaboration and policy alignmentMecomed, the Medical Technology Association in the Middle East and Africa, and MedTech Europe, a European trade association, held a joint event during WHX Dubai to promote collaboration and policy alignment in the MedTech industry. The discussions focused on innovation, regulation, and global-regional cooperation crucial for advancing medical technology in the Middle East and Africa, with the regional medical devices market expected to reach nearly USD 35 billion by 2032.EuractivCommission eyes lifting AI rules for medical devices after internal power struggleThe European Commission has proposed to exempt medical devices from many of the safety obligations under the EU’s AI Act, a move that has sparked internal divisions between EU directorates and criticism from some lawmakers regarding patient safety. The proposal aims to streamline compliance by allowing companies to rely on existing sector-specific rules until secondary legislation is adopted, a shift welcomed by industry groups like MedTech Europe and COCIR. Despite industry support, critics argue the change creates a regulatory gap for AI-driven medical technologies before the AI Act fully takes effect.RapsEuropean Commission publishes implementing regulation on conformity assessments by notified bodiesThe European Commission published an implementing regulation establishing uniform quality management and procedural requirements for conformity assessment activities conducted by notified bodies under the Medical Devices Regulation and In Vitro Diagnostic Regulation. The regulation, which takes effect on 25 February 2027, mandates specific timelines including 30 days for application review, 120 days for quality management system audits, 90 days for technical documentation assessment, and 20 days for certification decisions, addressing longstanding inconsistent practices among notified bodies. MedTech Europe welcomed the regulation as a timely step toward greater predictability, transparency, and consistency in conformity assessment that supports patient access and Europe's innovation capacity.