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Gummihandgriff

EUDAMED

Class I (EU MDR)

Ref BK 130Model Rubber-Handle

by Dr. Jean Bausch GmbH & Co. KG

Identity

Trade Name
Gummihandgriff EUDAMED
Model / Reference
Rubber-Handle EUDAMED
BK 130 EUDAMED

Identifiers

Primary DI / UDI-DI
+E210BK13018 EUDAMED
Basic UDI-DI
++E2105x1xRubberHandleRL EUDAMED
EMDN Code
Q010299 PROSTHETIC DENTISTRY DEVICES - 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

Gummihandgriff by Dr. Jean Bausch 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-000005577

Sources (1)

  • EUDAMED c6609032-f37c-4e64-9025-6514d4888aea 61 fields · synced Oct 6, 2026