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KS-S401fs

EUDAMED

Class I (EU MDR)

Ref KS-S401fsModel KS-S401fs, KS-S402fs, KS-S403fs, KS-S405fs, KS-S406fs, KS-S407fs, KS-S408fs, KS-S409fs, KS-S410fs, KS-S411fs, KS-S412fs, KS-S413fs, KS-S415fs, KS-S416fs, KS-S417fs, KS-S418fs, KS-S419fs, KS-S420fs

by Guangdong Kangshen Medical Technology Co., Ltd

Identity

Trade Name
KS-S401fs EUDAMED
Device Name
Manual Obstetric Bed EUDAMED
Model / Reference
KS-S401fs, KS-S402fs, KS-S403fs, KS-S405fs, KS-S406fs, KS-S407fs, KS-S408fs, KS-S409fs, KS-S410fs, KS-S411fs, KS-S412fs, KS-S413fs, KS-S415fs, KS-S416fs, KS-S417fs, KS-S418fs, KS-S419fs, KS-S420fs EUDAMED
KS-S401fs EUDAMED

Identifiers

Primary DI / UDI-DI
16979079130059 EUDAMED
Basic UDI-DI
697907913KS-S401fsPC EUDAMED
Direct Marketing DI
16979079130059 EUDAMED
EMDN Code
V080602 MANUAL MEDICAL BEDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

KS-S401fs by Guangdong Kangshen Medical Technology 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-000023814
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 8fc6ae71-7d0a-4753-8aed-9ebc2cb73930 61 fields · synced Jun 19, 2026