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Verdant

FDA UDI

Class I (US FDA UDI)

by Tranzonic Acquisition Corp.

Identity

Trade Name
Verdant FDA UDI
Generic Name
Polychloroprene examination/treatment glove, non-powdered FDA UDI
Device Name
Verdant Disposable Chloroprene Examination Grade Gloves, Powder Free, Green, XLarge, 100/bx, 10bx/cs FDA UDI
Model / Reference
GL-CR106GFX FDA UDI
Description
Verdant Disposable Chloroprene Examination Grade Gloves, Powder Free, Green, XLarge, 100/bx, 10bx/cs FDA UDI

Identifiers

Catalog Number
GL-CR106GFX FDA UDI
Primary DI / UDI-DI
00075289232282 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Polychloroprene 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polychloroprene examination/treatment glove, non-powdered

Verdant by Tranzonic Acquisition Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2ac17558-afad-4435-9e76-a787c3a37f3f 35 fields · synced May 30, 2026