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Dealmed

FDA UDI

Class I (US FDA UDI)

by Dealmed Medical Supplies Llc

Identity

Trade Name
Dealmed FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
Glove Exam Vinyl N/S PF X-Large Natural, 100/Bx FDA UDI
Model / Reference
787290 FDA UDI
Description
Glove Exam Vinyl N/S PF X-Large Natural, 100/Bx FDA UDI

Identifiers

Catalog Number
787290 FDA UDI
Primary DI / UDI-DI
00859140003460 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Vinyl 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

Dealmed by Dealmed Medical Supplies Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vinyl examination/treatment glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dealmed Medical Supplies Llc

Sources (1)

  • FDA UDI 9e5b5829-0b6b-4a82-8d88-2b6c5a1508cd 35 fields · synced Jun 8, 2026