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Unico – Kit Percutaneo Ch 12

EUDAMED

Class IIa (EU MDR)

Ref 10801Model 10800

by Redax S.p.A.

Identity

Trade Name
UNICO – KIT PERCUTANEO CH 12 EUDAMED
Device Name
UNICO - PERCUTANEOUS KIT CH 9 EUDAMED
Model / Reference
10800 EUDAMED
10801 EUDAMED

Identifiers

Primary DI / UDI-DI
08034139295602 EUDAMED
Basic UDI-DI
803413929UNICO1aRF EUDAMED
EMDN Code
A060204 THORACENTESIS AND PARACENTESIS DRAINAGES AND KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Unico – Kit Percutaneo Ch 12 by Redax S.p.A. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Redax S.p.A.
EUDAMED SRN
IT-MF-000019320

Sources (1)

  • EUDAMED fbeaa709-78c4-4a3b-9190-66ea407b3a1f 61 fields · synced Jul 11, 2026