VYGON Germany GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000005305 FEI 3002808464
- Devices
- 410
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
What VYGON Germany GmbH makes
VYGON Germany GmbH manufactures central venous catheterization kits for short-term use, including products such as splitneedle, premistar, multicath3, leadercathexpert, multicath2, multicath2expert UP, and multicath5expert.
These devices are classified as Class III and Class IIa and are listed in the EUDAMED registry. The company is based in Germany.
Catalogue
Search and filter all 410 devicesShowing 101-150 of 410
Company details
- EUDAMED SRN
- DE-MF-000005305
- FDA FEI number
- 3002808464
- EU VAT number
- DE121686446
- EUDAMED status
- Active
- EUDAMED registered name
- VYGON Germany GmbH
- EUDAMED abbreviated name
- VYGON Germany GmbH
- Registered address
- 100, Prager Ring, 52070, Aachen, Germany
- Website
- www.vygon.de
- facebook.com/VygonDeutschland
- [email protected]
- Phone
- +4924191300
- PRRC contact
- Bernd Marx
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 29 Jun 2030
BSI Group The Netherlands B.V. 2797 1 certificate
- MDR 817414 Active
Quality management system EU MDR
- Issued
- 21 Sep 2026
- Expires
- 29 Jun 2030
- Reason
- Change approved