Authorised Representative Active
mdi Europa GmbH
DE· DE-AR-000006218
Organization Details
- Legal Name
- mdi Europa GmbH
- Country
- DE
- SRN (Actor ID)
- DE-AR-000006218
- Status
- Active
- VAT Number
- DE812962943
- PRRC Contact
- Michael Sander
Contact Information
Langenhagen
30855
Registration Status
EUDAMED Status Active
Verified by deviCERTS Yes
Manufacturers represented
48- A-SPINE Asia Co., Ltd. — TW
- ARANZ MEDICAL LIMITED — NZ
- Accumax Lab Devices Private Limited — IN
- Air Kinetic Technologies Corp. — TW
- BESMED HEALTH BUSINESS CORP. — TW
- BLUE SKY BIO LLC — US
- Bio-Molecular Systems Pty Ltd — AU
- Black Box Voice Medical Ltd. — IL
- C-A-T Resources, LLC — US
- Co-Diagnostics, Inc. — US
- DAS MEDICAL INTERNATIONAL, SRL — DO
- DONG-A CHAMMED CO., LTD. — KR
- Daiwha Corp., Ltd. — KR
- Dongguan Concord Medical Products Ltd — CN
- EPSILON HEALTHCARE SOLUTIONS PRIVATE LIMITED — IN
- Excellent Hi -Care Private Limited — IN
- Flexmedics — US
- Genetic Signatures Ltd — AU
- Harsoria Healthcare Pvt. Ltd. — IN
- Hsiner Co., Ltd. — TW
- Infinite Biomedical Technologies LLC — US
- Invent Bio-Med Pvt Ltd — IN
- KEISEI MEDICAL INDUSTRIAL CO., LTD. — JP
- MEDICAL TECHNOLOGIES Ltd — RU
- Mediplus (India) Limited — IN
- NOVOXEL LTD — IL
- Nasus Pharma Ltd. — IL
- Nidek Medical Products Inc. — US
- Novamedic Co., Ltd. — TH
- Ortho Organizers, Inc. — US
- PRIMED MEDICAL PRODUCTS INC. — CA
- PROFESSIONAL LATEX SDN BHD — MY
- Pacific Hospital Supply Co., Ltd. — TW
- Point Designs, LLC — US
- Precision Biosensor Inc. — KR
- RAD SOURCE TECHNOLOGIES, INC. — US
- RRR Manufacturing Pty Ltd — AU
- Rhythmlink International, LLC — US
- SigTuple Technologies Pvt Ltd — IN
- TBG Biotechnology Corp. — TW
- Taiwan Advanced Nanotech Inc. — TW
- ToLife Technologies Pty. Ltd. — AU
- UNIQUE INTERNATIONAL SAS — CO
- Unimax Medical Systems Inc. — TW
- United Orthopedic Corporation — TW
- Viet Glove Corporation — VN
- World Class Technology Corporation — US
- YTY INDUSTRY SDN BHD — MY
Compliance Notice
This actor is registered as a Authorised Representative under EU Regulation 2017/745 (MDR) or 2017/746 (IVDR).
Last verified via EUDAMED integration.