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Kit Resettoscopia/Revisione/Isterescopia

EUDAMED

Class IIa (EU MDR)

Ref C03GYN0015Model Pacchi procedurali per Ginecologia – Sterile procedural packs for Gynecology

by Surgika srl

Identity

Trade Name
KIT RESETTOSCOPIA/REVISIONE/ISTERESCOPIA EUDAMED
Model / Reference
Pacchi procedurali per Ginecologia – Sterile procedural packs for Gynecology EUDAMED
C03GYN0015 EUDAMED

Identifiers

Primary DI / UDI-DI
08053178797076 EUDAMED
Basic UDI-DI
805961777PPSGYNXQ 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

Kit Resettoscopia/Revisione/Isterescopia 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 63b3b010-55b5-41bb-82cc-70ab8f932c36 61 fields · synced Jul 9, 2026