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HoverSling® Repositioning Sheet
EUDAMEDFDA UDIClass I (EU MDR)
Ref HMSLING-50RS-BModel Lateral Transfer Device
Identity
- Trade Name
- HoverSling® Repositioning Sheet EUDAMEDHoverSling Repositiong Sling FDA UDI
- Generic Name
- Patient transfer system, powered FDA UDI
- Device Name
- 50" Single Patient Use Repositioning HoverSling Breathable FDA UDI
- Model / Reference
- Lateral Transfer Device EUDAMEDHMSLING-50RS-B EUDAMEDFDA UDI
- Description
- 50" Single Patient Use Repositioning HoverSling Breathable FDA UDI
Identifiers
- Catalog Number
- HMSLING-50RS-B FDA UDI
- Primary DI / UDI-DI
- 00816299010596 EUDAMEDFDA UDI
- Basic UDI-DI
- 81629901REPOV2 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 — 50 Inch FDA UDI
HoverSling® Repositioning Sheet 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 | 81629901REPOV2 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- HoverTech International
- EUDAMED SRN
- US-MF-000008435
- Authorised Representative
- Etac Supply Center AB SE-AR-000001601
Sources (2)
- EUDAMED 6baf0519-9faf-437a-82a5-be36bed85e02 61 fields · synced Jul 9, 2026
- FDA UDI 2d741744-a094-41fa-8e25-4fc38dfc9441 37 fields · synced May 30, 2026