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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
Professional examination gown, single-use FDA UDI
Device Name
Top Scrub Hemmed Three-Pocket V-Neck Open 2X Large Spunbond Meltblown Spunbond Dark Blue Disposable Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference
DST2XL FDA UDI
Description
Top Scrub Hemmed Three-Pocket V-Neck Open 2X Large Spunbond Meltblown Spunbond Dark Blue Disposable Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI
50885632102897 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Professional examination gown, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

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: Professional examination gown, single-use

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

Similar devices

Also classified as Professional examination gown, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eb13bd00-9557-4427-8926-394d06640b9d 34 fields · synced Jun 8, 2026