Identity
- Trade Name
- BIODEL EUDAMED
- Device Name
- BIODEGRADABLE NITRILE POWDER FREE EXAMINATION GLOVES EUDAMED
- Model / Reference
- BIODEL EUDAMEDPPMD03EU EUDAMED
Identifiers
- Primary DI / UDI-DI
- 00860011343813 EUDAMED
- Basic UDI-DI
- 08600113438BIODELNGCQ EUDAMED
- EMDN Code
- T01020204 NITRILE EXAMINATION / TREATMENT GLOVES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium 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
Biodel by Medzah Industries — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 08600113438BIODELNGCQ | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medzah Industries
- EUDAMED SRN
- US-MF-000039359
- Authorised Representative
- Specculo Limited MT-AR-000034988
Sources (1)
- EUDAMED 7d640e7e-64ae-43d8-b2a9-2313fae88203 61 fields · synced May 22, 2026