Identity
- Device Name
- LUGOL NEITUM EUDAMED
- Model / Reference
- 851 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760274510151 EUDAMED
- Basic UDI-DI
- B-03760274510151 EUDAMED
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
Category: Device sterilization/disinfection container, reusable
Lugol Neitum by Laboratoires FRILAB — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
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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-03760274510151 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Laboratoires FRILAB
- EUDAMED SRN
- FR-MF-000013603
Sources (1)
- EUDAMED c8589e13-b621-48dc-8405-0041b82b8fa8 61 fields · synced Jun 18, 2026