← Back to catalogue
Single Patient Use HoverMatt
EUDAMEDFDA UDIClass I (EU MDR)
Ref HM39SPU-BModel Lateral Transfer Device
Identity
- Trade Name
- Single Patient Use HoverMatt EUDAMEDFDA UDI
- Generic Name
- Patient transfer system, powered FDA UDI
- Device Name
- 39" Single Patient Use HoverMatt Breathable FDA UDI
- Model / Reference
- Lateral Transfer Device EUDAMEDHM39SPU-B EUDAMEDFDA UDI
- Description
- 39" Single Patient Use HoverMatt Breathable FDA UDI
Identifiers
- Catalog Number
- HM39SPU-B FDA UDI
- Primary DI / UDI-DI
- 00816299010800 EUDAMEDFDA UDI
- Basic UDI-DI
- 081629901HMSM EUDAMED
- FDA Product Code
- FRZ FDA UDI
- EMDN Code
- V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
- GMDN Term
- Patient transfer system, powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.6775 FDA UDI
- Market of Registration
- Sweden 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Width — 34 Inch FDA UDI
Single Patient Use HoverMatt by Hovertech International — 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 | 081629901HMSM | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- HoverTech International
- EUDAMED SRN
- US-MF-000008435
- Authorised Representative
- Etac Supply Center AB SE-AR-000001601
Sources (2)
- EUDAMED 66defcbe-a3e8-4d91-bd2c-6f350d49e664 61 fields · synced Jun 6, 2026
- FDA UDI 26431aa8-f552-48cd-9221-e075d9559882 37 fields · synced May 30, 2026