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Arti-Check®

EUDAMED

Class I (EU MDR)

Ref BK 62Model Arti-Check®

by Dr. Jean Bausch GmbH & Co. KG

Identity

Trade Name
Arti-Check® EUDAMED
Model / Reference
Arti-Check® EUDAMED
BK 62 EUDAMED

Identifiers

Primary DI / UDI-DI
+E210BK621C EUDAMED
Basic UDI-DI
++E2101x4xArtiCheckx404J EUDAMED
Unit of Use DI
+E210BK620B EUDAMED
EMDN Code
Q01020201 ARTICULATION PAPERS 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

Arti-Check® 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 efb88031-97be-433e-bb5f-b29ef4e2329b 61 fields · synced Jun 19, 2026