← Back to catalogue

LiteGait

FDA UDI

Class I (US FDA UDI)

by Mobility Research

Identity

Trade Name
LiteGait FDA UDI
Generic Name
Gait rehabilitation system harness FDA UDI
Device Name
LiteGait is a Physical Therapy Patient lifting device that allows for body weight support gait therapy. FDA UDI
Model / Reference
ALL LiteGait devices FDA UDI
Description
LiteGait is a Physical Therapy Patient lifting device that allows for body weight support gait therapy. FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00850040235012 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Gait rehabilitation system harness 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: Gait rehabilitation system harness

LiteGait by Mobility Research — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gait rehabilitation system harness.

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
Mobility Research

Sources (1)

  • FDA UDI 887b8cd9-3620-4be2-8c83-38f8814c2c31 35 fields · synced May 29, 2026