Identity
- Trade Name
- KD-FINE BLUNT EUDAMED
- Device Name
- KD-FINE BLUNT EUDAMED
- Model / Reference
- 920282 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 24031881920286 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- KD Medical GmbH Hospital Products
- EUDAMED SRN
- DE-MF-000006773
Sources (1)
- EUDAMED d3e41819-d1bb-4ce5-8beb-5e25e44870f5 61 fields · synced Oct 7, 2026