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Alternating pressure air flotation mattress
EUDAMEDClass I (EU MDR)
Ref KE-917AH
Identity
- Trade Name
- Alternating pressure air flotation mattress EUDAMED
- Device Name
- Alternating pressure air flotation mattress EUDAMED
- Model / Reference
- KE-917AH EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04527799704514 EUDAMED
- Basic UDI-DI
- 4527799TD73D0120094 EUDAMED
- EMDN Code
- V080701 ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED
Classification
- Device Class
- Class I EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
Alternating pressure air flotation mattress by Paramount Bed 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 | 4527799TD73D0120094 | Class I | Active |
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Manufacturer
- Manufacturer
- Paramount Bed Co., Ltd.
- EUDAMED SRN
- JP-MF-000002285
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (1)
- EUDAMED 0a4df596-0aea-4a40-82ec-d6776d561fb1 61 fields · synced Jun 18, 2026