Identity
- Device Name
- Day-Use Pump Part (DUPP) EUDAMED
- Model / Reference
- 5201-62 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05907595122467 EUDAMED
- Basic UDI-DI
- 5907595122PV-5201DUPP7E EUDAMED
- EMDN Code
- A030499 ADMINISTRATION KITS - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
Yes
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
Yes
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Day-Use Pump Part (DUPP) by Vimex Sp. z o.o. — Class IIa — 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 | 5907595122PV-5201DUPP7E | Class IIa | Active |
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Manufacturer
- Manufacturer
- Vimex Sp. z o.o.
- EUDAMED SRN
- PL-MF-000008668
Sources (1)
- EUDAMED 1816f415-7e07-4687-9bdd-bd7aa9112828 61 fields · synced Jul 13, 2026