Identity
- Trade Name
- Intraocular Diathermy Probe EUDAMED
- Device Name
- Reusable Bipolar Instruments EUDAMED
- Model / Reference
- D8203 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04058935010102 EUDAMED
- Basic UDI-DI
- B-04058935010102 EUDAMED
- EMDN Code
- L031306 HEMOSTATIC FORCEPS, REUSABLE EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Netherlands EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Intraocular Diathermy Probe by Bausch & Lomb GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04058935010102 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Bausch & Lomb GmbH
- EUDAMED SRN
- DE-MF-000009142
Sources (1)
- EUDAMED 04e4f8bf-42f5-446a-a794-f03fbd2332ba 61 fields · synced Jul 18, 2026