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OccluSense®

EUDAMED

Class I (EU MDR)

Ref BK 5035Model OccluSense-Sensor

by Dr. Jean Bausch GmbH & Co. KG

Identity

Trade Name
OccluSense® EUDAMED
Model / Reference
OccluSense-Sensor EUDAMED
BK 5035 EUDAMED

Identifiers

Primary DI / UDI-DI
+E210BK50351H EUDAMED
Basic UDI-DI
++E21010x1xOSSensorJ2 EUDAMED
EMDN Code
Q01020299 DENTAL CONTACT INDICATORS - 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

OccluSense® 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 66caa582-da6d-4c95-8dc0-c0936db1a32f 61 fields · synced Oct 5, 2026