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Ks-S301et

EUDAMED

Class I (EU MDR)

Ref KS-S301ETModel KS-S301ET, KS-S302ET, KS-S303ET, KS-S305ET, KS-S306ET, KS-S307ET.KS-S308ET, KS-S309ET, KS-S310ET, KS-S311ET, KS-S312ET, KS-S313ET, KS-S315ET, KS-S316ET, KS-S317ET, KS-S318ET, KS-S319ET, KS-S320ET,

by Guangdong Kangshen Medical Technology Co., Ltd

Identity

Trade Name
KS-S301ET EUDAMED
Device Name
Manual Three Function Pediatric Hospital Bed EUDAMED
Model / Reference
KS-S301ET, KS-S302ET, KS-S303ET, KS-S305ET, KS-S306ET, KS-S307ET.KS-S308ET, KS-S309ET, KS-S310ET, KS-S311ET, KS-S312ET, KS-S313ET, KS-S315ET, KS-S316ET, KS-S317ET, KS-S318ET, KS-S319ET, KS-S320ET, EUDAMED
KS-S301ET EUDAMED

Identifiers

Primary DI / UDI-DI
06979079130212 EUDAMED
Basic UDI-DI
697907913M3FPHBQ7 EUDAMED
Direct Marketing DI
06979079130212 EUDAMED
EMDN Code
V080602 MANUAL MEDICAL BEDS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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-S301et 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 58863841-6190-4ab8-b2c3-62896dab045b 61 fields · synced Jul 13, 2026