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Buck

EUDAMED

Class I (EU MDR)

Ref 1-350 RI

by Raydent Instruments

Identity

Trade Name
BUCK EUDAMED
Device Name
BUCK EUDAMED
Model / Reference
1-350 RI EUDAMED

Identifiers

Primary DI / UDI-DI
G2681350RI0 EUDAMED
Basic UDI-DI
++G2681350RIC2 EUDAMED
EMDN Code
L160101 NEUROLOGICAL HAMMERS, 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

Buck by Raydent Instruments — 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
Raydent Instruments
EUDAMED SRN
PK-MF-000032781
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED f06f50a2-49bc-41c1-b0b8-993a97aedf26 61 fields · synced Jun 18, 2026