← Back to catalogue

Arti-Check®

EUDAMED

Class I (EU MDR)

Ref BK 13Model Arti-Check®

by Dr. Jean Bausch GmbH & Co. KG

Identity

Trade Name
Arti-Check® EUDAMED
Model / Reference
Arti-Check® EUDAMED
BK 13 EUDAMED

Identifiers

Primary DI / UDI-DI
+E210BK1318 EUDAMED
Basic UDI-DI
++E2101x4xArtiCheckx404J 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005577

Sources (1)

  • EUDAMED d4ac4b09-fa97-47aa-994c-4a0f6c1a0c30 61 fields · synced Oct 7, 2026