Identity
- Trade Name
- GoLift FDA UDI
- Generic Name
- Overhead track patient lifting/transfer system FDA UDI
- Device Name
- Patient Lift Quick Release Trolley Assembly - BHM FDA UDI
- Model / Reference
- GoLift Trolley FDA UDI
- Description
- Patient Lift Quick Release Trolley Assembly - BHM FDA UDI
Identifiers
- Catalog Number
- GO-LIFT-QR-TRLY-BHM-ASSY FDA UDI
- Primary DI / UDI-DI
- 00840722000328 FDA UDI
- FDA Product Code
- FSA FDA UDI
- GMDN Term
- Overhead track patient lifting/transfer system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5510 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: Overhead track patient lifting/transfer system
GoLift by Amico Mobility Solutions Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Amico Mobility Solutions Corporation
Sources (1)
- FDA UDI e39e43b9-0cf5-443c-b5c3-c0e16c302929 36 fields · synced May 31, 2026