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UDI Compass
Unknown / Not in EUDAMED

Snapshot 2026-10-09 · Link to EUDAMED

AphtoFix

UDI-DI 07611645209005Basic UDI-DI 7611645AP0700GG

Class IIa · MDR · bonyf AG

Identification
Model
—
Issuing agency
GS1
Device status
active
Sterile
No
Implantable
No
Measuring function
No
Reusable surgical
No
Certificates

50537-60-00-03

EU quality management system · unknown

Notified body: DEKRA Certification GmbH (0124)

Valid from 2026-07-30 · Expiry 2027-04-18

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

bonyf AG

SRN LI-MF-000000739

LI · Vaduz

manufacturer

Related UDI-DIs

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/aphtofix-9005 · UDI page: /udi/07611645209005

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