Identity
- Trade Name
- Bimeo PRO EUDAMED
- Device Name
- Bimeo PRO EUDAMED
- Model / Reference
- KNBM0001 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03830079450003 EUDAMED
- Basic UDI-DI
- 383007945BIMEO86 EUDAMED
- Direct Marketing DI
- 03830079450003 EUDAMED
- EMDN Code
- Y0504 ARMS, TORSO AND LEGS RE-EDUCATION DEVICES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Slovenia 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
Category: Rubber dam, Hevea-latex
Bimeo PRO by Kinestica d.o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Rubber dam, Hevea-latex.
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 383007945BIMEO86 | Class I | Active |
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Manufacturer
- Manufacturer
- Kinestica d.o.o.
- EUDAMED SRN
- SI-MF-000003773
Sources (1)
- EUDAMED f7ff15bd-630f-4b68-aaa5-3bd6a6f8e76b 61 fields · synced Oct 6, 2026