Identity
- Trade Name
- Kirofix Medium EUDAMED
- Device Name
- KIROFIX AND ACCESSORIES EUDAMED
- Model / Reference
- 0226-03-00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03700751500343 EUDAMED
- Basic UDI-DI
- 3700751502266E EUDAMED
- EMDN Code
- V0804 PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures) EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Kirofix Medium by Askorn Medical — 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 | 3700751502266E | Class I | Active |
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Manufacturer
- Manufacturer
- Askorn Medical
- EUDAMED SRN
- FR-MF-000001716
Sources (1)
- EUDAMED 1dc51ad0-5dac-4ba2-8d2f-e3b6bd8396e3 61 fields · synced Jul 14, 2026