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Ks-S001et
EUDAMEDClass I (EU MDR)
Ref KS-S001ETModel KS-S001ET, KS-S002ET, KS-S003ET, KS-S005ET, KS-S006ET, KS-S007ET, KS-S008ET, KS-S009ET, KS-S010ET, KS-S011ET, KS-S012ET, KS-S013ET, KS-S015ET, KS-S016ET, KS-S017ET, KS-S018ET, KS-S019ET, KS-S020ET
Identity
- Trade Name
- KS-S001ET EUDAMED
- Device Name
- Manual Flat Pediatric Hospital Bed EUDAMED
- Model / Reference
- KS-S001ET, KS-S002ET, KS-S003ET, KS-S005ET, KS-S006ET, KS-S007ET, KS-S008ET, KS-S009ET, KS-S010ET, KS-S011ET, KS-S012ET, KS-S013ET, KS-S015ET, KS-S016ET, KS-S017ET, KS-S018ET, KS-S019ET, KS-S020ET EUDAMEDKS-S001ET EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06979079130236 EUDAMED
- Basic UDI-DI
- 697907913MFPHBTG EUDAMED
- Direct Marketing DI
- 06979079130236 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-S001et 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 697907913MFPHBTG | Class I | Active |
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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 (1)
- EUDAMED 3982b0d0-2aa0-4332-be1d-c5c961910206 61 fields · synced Jul 22, 2026