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Reflex Hammer

EUDAMED

Class I (EU MDR)

Ref M1.121.312

by Luxamed GmbH & Co. KG

Identity

Device Name
Reflex Hammer EUDAMED
Model / Reference
M1.121.312 EUDAMED

Identifiers

Primary DI / UDI-DI
04260381963721 EUDAMED
Basic UDI-DI
426038196ReflexhammerC6 EUDAMED
EMDN Code
L160199 DIAGNOSTIC HAMMERS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Reflex Hammer by Luxamed GmbH & Co. KG — 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

EUDAMED SRN
DE-MF-000006437

Sources (1)

  • EUDAMED 40bf67a5-f8fe-4adb-8064-a26e9303f410 61 fields · synced Jun 19, 2026