Identity
- Trade Name
- K-Zoem EUDAMEDK-Zoem EZ-TURN FDA UDI
- Generic Name
- Low-air-loss bed FDA UDI
- Device Name
- K-Zoem EZ-TURN EUDAMEDLateral Rotation with True Low Air Loss Mattress System, 80" x 36" x 10" FDA UDI
- Model / Reference
- K-Zoem EUDAMEDK-ZoemMS FDA UDI
- Description
- Lateral Rotation with True Low Air Loss Mattress System, 80" x 36" x 10" FDA UDI
Identifiers
- Catalog Number
- K-ZoemMS FDA UDI
- Primary DI / UDI-DI
- 00817012021806 EUDAMEDFDA UDI
- Basic UDI-DI
- 081701202KZoemC8 EUDAMED
- Direct Marketing DI
- 00817012021806 EUDAMED
- FDA Product Code
- IKZ FDA UDI
- EMDN Code
- V080701 ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES EUDAMED
- GMDN Term
- Low-air-loss bed FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 890.5225 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
K-Zoem by Kap Medical — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 081701202KZoemC8 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- KAP Medical
- EUDAMED SRN
- US-MF-000007868
- Authorised Representative
- Obelis s.a. BE-AR-000000106
Sources (2)
- EUDAMED a75f3788-f3a4-4c12-93ee-9bc80b242f3b 61 fields · synced Jul 17, 2026
- FDA UDI 53558c5d-988e-4cde-ba97-f1fa4858ee02 35 fields · synced May 30, 2026