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KS-S501fs
EUDAMEDClass I (EU MDR)
Ref KS-S501fsModel KS-S501fs、KS-S502fs、KS-S503fs、KS-S505fs、KS-S506fs、KS-S507fs、KS-S508fs、KS-S509fs、KS-S510fs、KS-S511fs、KS-S512fs、KS-S513fs、KS-S515fs、KS-S516fs、KS-S517fs、KS-S518fs、KS-S519fs、KS-S520fs
Identity
- Trade Name
- KS-S501fs EUDAMED
- Device Name
- Manual Operating Table EUDAMED
- Model / Reference
- KS-S501fs、KS-S502fs、KS-S503fs、KS-S505fs、KS-S506fs、KS-S507fs、KS-S508fs、KS-S509fs、KS-S510fs、KS-S511fs、KS-S512fs、KS-S513fs、KS-S515fs、KS-S516fs、KS-S517fs、KS-S518fs、KS-S519fs、KS-S520fs EUDAMEDKS-S501fs EUDAMED
Identifiers
- Primary DI / UDI-DI
- 16979079130172 EUDAMED
- Basic UDI-DI
- 697907913KS-S501yhQS EUDAMED
- Direct Marketing DI
- 16979079130172 EUDAMED
- EMDN Code
- V080602 MANUAL MEDICAL BEDS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy 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-S501fs 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 | 697907913KS-S501yhQS | 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 72620876-db1f-4fcd-b4c0-f4ee2ae7d78a 61 fields · synced Jul 22, 2026