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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Ethylene vinyl acetate examination/treatment glove, non-powdered FDA UDI
Device Name
GLOVE,EXAM,VINYL,STERILE,PF,LF,SGL,MD FDA UDI
Model / Reference
484402 FDA UDI
Description
GLOVE,EXAM,VINYL,STERILE,PF,LF,SGL,MD FDA UDI

Identifiers

Catalog Number
484402 FDA UDI
Primary DI / UDI-DI
30080196994933 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Ethylene vinyl acetate examination/treatment glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ethylene vinyl acetate examination/treatment glove, non-powdered

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

Similar devices

Also classified as Ethylene vinyl acetate examination/treatment glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 1207d740-1147-41bb-ae2b-095d9d98993e 36 fields · synced Jun 1, 2026