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Check Retractor

EUDAMED

Class I (EU MDR)

Ref C SeriesModel ”C” Series, “M”Series, “Y”Series, “O”Series, Double-headed Series

by Changzhou Shengkang Medical Instrument Co., Ltd.

Identity

Device Name
Check Retractor EUDAMED
Model / Reference
”C” Series, “M”Series, “Y”Series, “O”Series, Double-headed Series EUDAMED
C Series EUDAMED

Identifiers

Primary DI / UDI-DI
06979853490501 EUDAMED
Basic UDI-DI
697985349CR001QX EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

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

Category: Device sterilization/disinfection container, reusable

Check Retractor by Changzhou Shengkang Medical Instrument Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000035829
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 99bef812-e564-4c32-8fa4-896315f66d88 61 fields · synced Oct 6, 2026