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Arti-Wax

EUDAMED

Class I (EU MDR)

Ref BK 6201Model Arti-WaxRef BK 6203

by Dr. Jean Bausch GmbH & Co. KG

Identity

Trade Name
Arti-Wax EUDAMED
Model / Reference
Arti-Wax EUDAMED
BK 6201 EUDAMED
BK 6203 EUDAMED

Identifiers

Primary DI / UDI-DI
+E210BK62011D EUDAMED
+E210BK62031F EUDAMED
Basic UDI-DI
++E21011x2x2xArtiWaxZS EUDAMED
Unit of Use DI
+E210BK62010C EUDAMED
+E210BK62030E EUDAMED
EMDN Code
Q01020203 OCCLUSAL WAXES 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-Wax 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 (2)

  • EUDAMED 0afd41f3-3837-4746-969a-2b173ef073ff 61 fields · synced Oct 6, 2026
  • EUDAMED 8c6661e9-2a10-4eb2-acf9-17e31bdca6bb 61 fields · synced May 18, 2026