Identity
- Trade Name
- Molift FDA UDI
- Generic Name
- Standing transfer platform, manual FDA UDI
- Model / Reference
- Molift Transfer Pro O-Bracket FDA UDI
Identifiers
- Catalog Number
- 1630040 FDA UDI
- Primary DI / UDI-DI
- 05707995038524 FDA UDI
- FDA Product Code
- IKX FDA UDI
- GMDN Term
- Standing transfer platform, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Standing transfer platform, manual
Molift by Etac A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Standing transfer platform, manual.
- Protekt Pilot — Proactive Medical Products · Class I
- Vancare Vanturn — VANCARE INC · Class I
- Vancare Vanturn — VANCARE INC · Class I
- Vancare Vanturn — VANCARE INC · Class I
- Protekt Pilot — Proactive Medical Products · Class I
- Molift — Etac A/S · Class I
- Molift — Etac A/S · Class I
- Molift — Etac A/S · 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
- Etac A/S
Sources (1)
- FDA UDI 211f1992-d169-4b6a-a85c-e7fc52c2e80b 33 fields · synced Jun 8, 2026