Identity
- Trade Name
- EUDAMED Test Artikel 3 EUDAMED
- Device Name
- EUDAMED Test Artikel 1 EUDAMED
- Model / Reference
- 405825 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04262526340275 EUDAMED
- Basic UDI-DI
- 4262526349995Z6 EUDAMED
- Direct Marketing DI
- 04262526340275 EUDAMED
- EMDN Code
- Z12030399 INFUSION INSTRUMENTS - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
EUDAMED Test Artikel 3 by provita medical gmbh & co. kg — 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 | 4262526349995Z6 | Class I | Active |
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Manufacturer
- Manufacturer
- provita medical gmbh & co. kg
- EUDAMED SRN
- DE-MF-000005332
Sources (1)
- EUDAMED c950f05a-1449-434b-88de-e14d9658d2e2 61 fields · synced Jun 18, 2026