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Beyer

EUDAMED

Class I (EU MDR)

Ref 12-879-18-07

by FHQ Trading CO.

Identity

Trade Name
Beyer EUDAMED
Device Name
Beyer EUDAMED
Model / Reference
12-879-18-07 EUDAMED

Identifiers

Primary DI / UDI-DI
G4381287918070 EUDAMED
Basic UDI-DI
++G438128791807JN EUDAMED
EMDN Code
L091302 BONE RONGEURS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Beyer by FHQ Trading CO. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
FHQ Trading CO.
EUDAMED SRN
PK-MF-000033179
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 012b691f-7d76-4a10-b4d7-e10b393852fb 61 fields · synced Jun 19, 2026