← Back to catalogue

Subiton CIFO

EUDAMED

Class IIa (EU MDR)

Ref 885005Model Martillo Quirúrgico

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
Martillo Quirúrgico EUDAMED
885005 EUDAMED

Identifiers

Primary DI / UDI-DI
07798034468042 EUDAMED
Basic UDI-DI
B-07798034468042 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

Subiton CIFO by Laboratorios SL S.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 8a43fe75-5d1c-458a-84cb-3f8ea3583bcf 61 fields · synced Aug 2, 2026