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VYGON Germany GmbH

Active in EUDAMED

Germanyfrom SRN EUDAMED FDA SRN DE-MF-000005305 FEI 3002808464

Devices
410
Registrations
EUDAMEDFDA
FDA recalls
0

Catalogue410

Newest first, page 2 of 9

Showing 51-100 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
Phone
+4924191300
PRRC contact
Bernd Marx(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 29 Jun 2030

EUDAMED certificates (1)

Notified body 2797 1 certificate

  • MDR 817414 Supplemented

    Quality management system EU MDR

    Issued
    21 Sep 2026
    Expires
    29 Jun 2030
    Reason
    Change approved

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.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.