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Derma Nytril Soft Nero
EUDAMEDClass I (EU MDR)
Ref 42573XLModel GUANTO IN NITRILE
Identity
- Trade Name
- DERMA NYTRIL SOFT NERO EUDAMED
- Device Name
- GUANTO MONOUSO IN NITRILE SENZA POLVERE EUDAMED
- Model / Reference
- GUANTO IN NITRILE EUDAMED42573XL EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08024151806399 EUDAMED
- Basic UDI-DI
- 8024151GUNSYY EUDAMED
- Direct Marketing DI
- 08024151806399 EUDAMED
- EMDN Code
- T01020204 NITRILE EXAMINATION / TREATMENT GLOVES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy 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
Derma Nytril Soft Nero by Bericah S.p.A. — 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 | 8024151GUNSYY | Class I | Active |
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Manufacturer
- Manufacturer
- Bericah S.p.A.
- EUDAMED SRN
- IT-MF-000007397
Sources (1)
- EUDAMED ea95fc67-deb5-42c7-8186-bc2d473e124b 61 fields · synced Jun 18, 2026