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MedNet EC-REP at CMEF Shanghai 2025 – Visit Us at Booth Hall 8.1 F39
We are pleased to announce that MedNet EC-REP GmbH will be exhibiting at the China International Medical Equipment Fair (CMEF) in Shanghai from April 8 to April 11, 2025. You can find us at Hall 8.1, Booth F39.
CMEF is Asia’s leading medical and health technology exhibition, attracting more than 4,000 exhibitors and 120,000 visitors from over 100 countries. The event provides a comprehensive platform for medical device manufacturers, regulatory experts, and healthcare professionals to explore the latest innovations, regulatory updates, and market opportunities in the global medtech industry.
As your reliable European Authorized Representative and Regulatory Importer, MedNet EC-REP supports non-EU manufacturers in achieving and maintaining compliance with European regulatory requirements. At CMEF, our team will be available to discuss how we can assist with EU market access and ongoing regulatory obligations.
We look forward to meeting our clients and partners - and to making new connections—during this key international industry event.
Schedule a meeting or simply stop by Hall 8.1, Booth F39 - we’re looking forward to seeing you in Shanghai!
Latest news
New MIR Form 7.3.1: Key Update for Incident Reporting under EU MDR
The European Commission has released a new version of the Manufacturer Incident Report (MIR) form which will become mandatory for all medical device manufacturers from November 2025.
EUDAMED Workshop: Essential Training for Medical Device Stakeholders
The European Commission is hosting a free, hybrid EUDAMED workshop in Stuttgart on May 21, 2025, designed to support the onboarding of all actors involved with the European Database on Medical Devices (EUDAMED).
EU Expands Harmonised Standards for MDR: Focus on Medical Gloves, Sterilisation, and Patient Transport Equipment
The European Commission has taken a significant step in strengthening the regulatory framework for medical devices by harmonising additional standards under the MDR.
New Revision of MDCG 2020-16 Guidance on IVD Classification: Key Updates in Version 4
The Medical Device Coordination Group (MDCG) has released Revision 4 of the "Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746" (MDCG 2020-16).
UK Updates Post-Market Surveillance Requirements for Medical Devices
The Medicines and Healthcare products Regulatory Agency (MHRA) has released updated guidance on post-market surveillance (PMS) requirements for medical devices in Great Britain.
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ISO 15223-1 Amendment: EC-REP Symbol Changes to EU-REP
The International Organization for Standardization (ISO) has recently amended ISO 15223-1:2021, introducing a change from "EC-REP" to "EU-REP" for the European Authorized Representative symbol.
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MedNet EC-REP at MedTec Japan 2025 – Meet Us at Booth 3303
We are pleased to announce our participation as an exhibitor at MedTec Japan 2025, one of Asia’s leading trade shows for medical device design and manufacturing. The event will take place in Tokyo from April 9–11, 2025.