Identity
- Trade Name
- KD-FINE BLUNT EUDAMED
- Device Name
- KD-FINE BLUNT EUDAMED
- Model / Reference
- 909300A EUDAMED
Identifiers
- Primary DI / UDI-DI
- 54031881909305 EUDAMED
- Basic UDI-DI
- 4031881G11-01IsMJ EUDAMED
- EMDN Code
- A019001 BLUNT NEEDLES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Sweden EUDAMED
Clinical & Handling
Sterile
Yes
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
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Kd-Fine Blunt by KD Medical GmbH Hospital Products — 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 | 4031881G11-01IsMJ | Class I | Active |
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Manufacturer
- Manufacturer
- KD Medical GmbH Hospital Products
- EUDAMED SRN
- DE-MF-000006773
Sources (1)
- EUDAMED 5dff6041-1ad6-48a9-b4bb-5dc5727bb8dd 61 fields · synced Jun 18, 2026