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KS-S001yh

EUDAMED

Class I (EU MDR)

Ref KS-S001yhModel KS-S001ph、KS-S002ph、KS-S003ph、KS-S005ph、KS-S006ph、KS-S007ph、KS-S008ph、KS-S009ph、KS-S010phModel KS-S001yh、KS-S002yh、KS-S003yh、KS-S005yh、KS-S006yh、KS-S007yh

by Guangdong Kangshen Medical Technology Co., Ltd

Identity

Trade Name
KS-S001yh EUDAMED
Device Name
Manual Examination Bed EUDAMED
Manual Flat Hospital Bed EUDAMED
Model / Reference
KS-S001ph、KS-S002ph、KS-S003ph、KS-S005ph、KS-S006ph、KS-S007ph、KS-S008ph、KS-S009ph、KS-S010ph EUDAMED
KS-S001yh EUDAMED
KS-S001yh、KS-S002yh、KS-S003yh、KS-S005yh、KS-S006yh、KS-S007yh EUDAMED

Identifiers

Primary DI / UDI-DI
06979079130243 EUDAMED
06979079130328 EUDAMED
Basic UDI-DI
697907913KS-S001phN8 EUDAMED
697907913KS-S001yhP3 EUDAMED
Direct Marketing DI
06979079130243 EUDAMED
06979079130328 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-S001yh 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

Manufacturer
Guangdong Kangshen Medical Technology Co., Ltd
EUDAMED SRN
CN-MF-000023814
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 913c4082-2982-42ad-9f53-4502dcffaafd 61 fields · synced Jul 22, 2026
  • EUDAMED c7a7bf3b-b598-406a-b78a-5d254bf10086 61 fields · synced May 16, 2026