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MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
MediChoice FDA UDI
Generic Name
Tubular support bandage, non-latex, reusable FDA UDI
Device Name
Bandage Tubular Elastic Support Natural Size I 5 1/2X11YDS Large Knee Xl Thigh Xs Trunk MediChoice FDA UDI
Model / Reference
TSB5550 FDA UDI
Description
Bandage Tubular Elastic Support Natural Size I 5 1/2X11YDS Large Knee Xl Thigh Xs Trunk MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
10885632145872 FDA UDI
FDA Product Code
MHW FDA UDI
GMDN Term
Tubular support bandage, non-latex, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Category: Tubular support bandage, non-latex, reusable

MediChoice by Owens & Minor Distribution, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Owens & Minor Distribution, Inc.

Sources (1)

  • FDA UDI 0483c506-8b4e-461d-bab4-0a026eb2a497 33 fields · synced Jun 8, 2026