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Suture Kits

EUDAMED

Class I (EU MDR)

Ref ST2800

by Hubei V-Medical Products Co., Ltd.

Identity

Trade Name
Suture Kits EUDAMED
Device Name
Suture Kits 消毒缝合包 EUDAMED
Model / Reference
ST2800 EUDAMED

Identifiers

Primary DI / UDI-DI
16942013203201 EUDAMED
Basic UDI-DI
697023378SutureKitsZN EUDAMED
Direct Marketing DI
06942013203204 EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Suture Kits by Hubei V-Medical Products Co., Ltd. — Class I — 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

EUDAMED SRN
CN-MF-000011268
Authorised Representative
RAFFIN MEDICAL FR-AR-000004632

Sources (1)

  • EUDAMED b21a1754-bdd3-4f3c-977f-59226fe84b6e 61 fields · synced Jun 19, 2026