← Back to catalogue

Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Wheelchair/chair/stander occupant restraint/support FDA UDI
Device Name
BELT,WRAP AROUND,BEIGE,2XL,HOOK&LOOP FDA UDI
Model / Reference
MDT36582XL FDA UDI
Description
BELT,WRAP AROUND,BEIGE,2XL,HOOK&LOOP FDA UDI

Identifiers

Catalog Number
MDT36582XL FDA UDI
Primary DI / UDI-DI
10888277673304 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Wheelchair/chair/stander occupant restraint/support FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair/chair/stander occupant restraint/support

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair/chair/stander occupant restraint/support.

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

Sources (1)

  • FDA UDI 9a467403-2bb8-45f6-a6a4-7617d4b1f3d6 35 fields · synced May 30, 2026