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Set Fimosi

EUDAMED

Class IIa (EU MDR)

Ref C03GEN0205Model Pacchi procedurali per Chirurgia Generale – Sterile procedural packs for General Surgery

by Surgika srl

Identity

Trade Name
SET FIMOSI EUDAMED
Model / Reference
Pacchi procedurali per Chirurgia Generale – Sterile procedural packs for General Surgery EUDAMED
C03GEN0205 EUDAMED

Identifiers

Primary DI / UDI-DI
08059617772499 EUDAMED
Basic UDI-DI
805961777PPSGENVU EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT 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

Set Fimosi by Surgika srl — 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
Surgika srl
EUDAMED SRN
IT-MF-000024206

Sources (1)

  • EUDAMED 78c5089a-d936-48e9-a15b-2e3b0b6a5200 61 fields · synced Jul 31, 2026