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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

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.

Catalogue410

Newest first, rows 401-410 of 410

Search and filter all 410 devices

  • premicath Ref 1261.208

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • multicath3 Ref 1231.123

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • multistar5 UP Ref 6159.272

    Active Regimes: CE MDD Registry: EUDAMED Class:III

  • splitneedle Ref 7366.910

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • premistar Ref 6261.20

    Active Regimes: CE MDD Registry: EUDAMED Class:III

  • multicath3 Ref 1233.083

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • leadercathexpert Ref 8128.620

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • multicath2 Ref 157.352

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • multicath2expert UP Ref 8157.372

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

  • multicath5expert Ref 8159.125

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa

Showing 401-410 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)

BSI Group The Netherlands B.V. 2797 1 certificate

  • MDR 817414 Active Supplemented

    Quality management system EU MDR

    Issued
    21 Sep 2026
    Expires
    29 Jun 2030
    Reason
    Change approved