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Subiton CIFO

EUDAMED

Class IIa (EU MDR)

Ref 881933Model Jeringa para inflado

by Laboratorios SL S.A.

Identity

Trade Name
Subiton CIFO EUDAMED
Device Name
Sistema estéril de cifoplastía por balón – Componentes del set EUDAMED
Model / Reference
Jeringa para inflado EUDAMED
881933 EUDAMED

Identifiers

Primary DI / UDI-DI
07798034461210 EUDAMED
Basic UDI-DI
B-07798034461210 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

Similar devices

Also classified as Intraosseous infusion kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
AR-MF-000023153
Authorised Representative
Synergie Ingénierie Médicale FR-AR-000001802

Sources (1)

  • EUDAMED fc1c3756-a0be-4ee4-871c-d97d56f595e5 61 fields · synced Jul 19, 2026