← Back to catalogue

GoLift

FDA UDI

Class I (US FDA UDI)

by Amico Mobility Solutions Corporation

Identity

Trade Name
GoLift FDA UDI
Generic Name
Overhead track patient lifting/transfer system FDA UDI
Device Name
GO LIFT 1000 CURTAIN JUMPING 7 AXLE TROLLEY FDA UDI
Model / Reference
GoLift Trolley FDA UDI
Description
GO LIFT 1000 CURTAIN JUMPING 7 AXLE TROLLEY FDA UDI

Identifiers

Catalog Number
GO-LIFT-1000-CJ-TRLY-7-ASY FDA UDI
Primary DI / UDI-DI
00840722000540 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

Similar devices

Also classified as Overhead track patient lifting/transfer system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Amico Mobility Solutions Corporation

Sources (1)

  • FDA UDI c4db5156-6c3c-4b82-b889-2df515fa0d36 36 fields · synced Jun 1, 2026