Identity
- Trade Name
- Handi-Move Slide FDA UDI
- Generic Name
- Patient transfer sliding mat FDA UDI
- Device Name
- Handi Slide padded mini FDA UDI
- Model / Reference
- 3606 00000001 FDA UDI
- Description
- Handi Slide padded mini FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05404016612588 FDA UDI
- FDA Product Code
- FMR FDA UDI
- GMDN Term
- Patient transfer sliding mat FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6785 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Patient transfer sliding mat
Handi-Move Slide by Handi-Move — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient transfer sliding mat.
- AirPal Repositioning Sheet — RENU MEDICAL, INC · Class I
- HoverTech Lateral Transfer Mat — RENU MEDICAL, INC · Class I
- Vive — VIVE HEALTH LLC · Class I
- AirPal Repositioning Sheet — RENU MEDICAL, INC · Class I
- Arjo Slides Sheet — Arjohuntleigh, Inc. · Class I
- Sage Lateral Transfer Mat — RENU MEDICAL, INC · Class I
- AirPal Repositioning Sheet — RENU MEDICAL, INC · Class I
- Arjo Slides Tube — Arjohuntleigh, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| 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
- Handi-Move
Sources (1)
- FDA UDI 7ea1806c-aacd-4c55-8a75-fe0483cead83 33 fields · synced May 30, 2026