← Back to catalogue

GoLift Portable 450

EUDAMEDFDA UDI

Class I (EU MDR)

Ref GoLift Portable 450

by Amico Mobility Solutions

Identity

Trade Name
GoLift Portable 450 EUDAMED
GoLift FDA UDI
Generic Name
Overhead track patient lifting/transfer system FDA UDI
Device Name
GoLift products EUDAMED
PORTABLE LIFT 450LB- AMICO (POWER SUPPLY EXCLUDED, HAND CONTROL INCLUDED) FDA UDI
Model / Reference
GoLift Portable 450 EUDAMED
GO-LIFT-PTB-450 FDA UDI
Description
PORTABLE LIFT 450LB- AMICO (POWER SUPPLY EXCLUDED, HAND CONTROL INCLUDED) FDA UDI

Identifiers

Catalog Number
GO-LIFT-PORT-450-WR FDA UDI
Primary DI / UDI-DI
00840722000120 EUDAMEDFDA UDI
Basic UDI-DI
684706572400699 EUDAMED
FDA Product Code
FSA FDA UDI
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS EUDAMED
GMDN Term
Overhead track patient lifting/transfer system FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5510 FDA UDI
Market of Registration
France 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

GoLift Portable 450 by Amico Mobility Solutions — 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

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

Manufacturer

EUDAMED SRN
CA-MF-000041669
Authorised Representative
AJW Technology Consulting GmbH DE-AR-000004999

Sources (2)

  • EUDAMED 3aa19373-8cbb-45a7-b6b2-3e6341c64341 61 fields · synced Aug 2, 2026
  • FDA UDI ecd4d17e-32f3-4a68-8620-a86ba4d1ad70 36 fields · synced May 30, 2026