Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: Medline FDA UDI
Generic Name: Gait rehabilitation system harness FDA UDI
Device Name: GAIT BELT,YELLOW,FALL MGMT,72" 1EA FDA UDI
Model / Reference: MDT821203YL FDA UDI
Description: GAIT BELT,YELLOW,FALL MGMT,72" 1EA FDA UDI

Identifiers

Catalog Number: MDT821203YL FDA UDI
Primary DI / UDI-DI: 10080196374779 FDA UDI
FDA Product Code: IKX FDA UDI
FMQ FDA UDI
GMDN Term: Gait rehabilitation system harness FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5050 FDA UDI
880.6760 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Gait rehabilitation system harness

Medline by Medline Industries, Inc. — 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: Medline Industries, Inc.

Sources (1)

FDA UDI fc545225-1638-4a92-9aab-eab136ab4bd1 35 fields · synced May 31, 2026