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Ks-S101et
EUDAMEDClass I (EU MDR)
Ref KS-S101ETModel KS-S101ET, KS-S102ET, KS-S103ET, KS-S105ET, KS-S106ET, KS-S107ET, KS-S108ET, KS-S109ET, KS-S110ET, KS-S111ET, KS-S112ET, KS-S113ET, KS-S115ET, KS-S116ET, KS-S117ET, KS-S118ET, KS-S119ET, KS-S120ET
Identity
- Trade Name
- KS-S101ET EUDAMED
- Device Name
- Manual One Function Pediatric Hospital Bed EUDAMED
- Model / Reference
- KS-S101ET, KS-S102ET, KS-S103ET, KS-S105ET, KS-S106ET, KS-S107ET, KS-S108ET, KS-S109ET, KS-S110ET, KS-S111ET, KS-S112ET, KS-S113ET, KS-S115ET, KS-S116ET, KS-S117ET, KS-S118ET, KS-S119ET, KS-S120ET EUDAMEDKS-S101ET EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06979079130205 EUDAMED
- Basic UDI-DI
- 697907913M1FPHBPH EUDAMED
- Direct Marketing DI
- 06979079130205 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-S101et 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 | 697907913M1FPHBPH | 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 411ad1c5-470e-40a6-b23b-1dd48c292060 61 fields · synced Jun 20, 2026