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bonyf AG

Liechtenstein LI-MF-000000739 Last updated 23 Oct 2026

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Devices
13
Registries
EUDAMEDFDA 510(k)FDA
FDA recalls
0

Catalogue13

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 0124 1 certificate

  • 50537-60-00-03 Supplemented

    Quality management system EU MDR

    Issued
    30 Jul 2026
    Expires
    18 Apr 2027
    Reason
    Other

Notified bodies

  • Notified body 0124

Information

Country
Liechtenstein
Address
16, Heiligkreuz, Vaduz, Liechtenstein
Website
www.bonyf.com
PRRC contact
Vait Cerkezi
EUDAMED SRN
LI-MF-000000739
FDA FEI number
6036