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Subiton CIFO
EUDAMEDClass IIa (EU MDR)
Ref 885003Model Alambre guía y porta alambres
Identity
- Trade Name
- Subiton CIFO EUDAMED
- Device Name
- Sistema estéril de cifoplastía por balón – Componentes del set EUDAMED
- Model / Reference
- Alambre guía y porta alambres EUDAMED885003 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07798034468035 EUDAMED
- Basic UDI-DI
- B-07798034468035 EUDAMED
- EMDN Code
- A019011 INTRAOSSEOUS INFUSION AND VERTEBROPLASTY INFUSION NEEDLES AND KITS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Category: Intraosseous infusion kit
Subiton CIFO by Laboratorios SL S.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-07798034468035 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Laboratorios SL S.A.
- EUDAMED SRN
- AR-MF-000023153
- Authorised Representative
- Synergie Ingénierie Médicale FR-AR-000001802
Sources (1)
- EUDAMED 086aab83-0db0-4892-b014-164134fc2871 61 fields · synced Jun 19, 2026