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Tronex International, Inc.

FDA UDI

Class I (US FDA UDI)

by Tronex International, Inc.

Identity

Trade Name
Tronex International, Inc. FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Glove, Exam, Nitrile, Sterile, Chemotherapy Rated, Fully Textured, 12", Powder-Free, Latex-Free Pair, Blue, Extra-Large FDA UDI
Model / Reference
9258STR-35 FDA UDI
Description
Glove, Exam, Nitrile, Sterile, Chemotherapy Rated, Fully Textured, 12", Powder-Free, Latex-Free Pair, Blue, Extra-Large FDA UDI

Identifiers

Primary DI / UDI-DI
20097604925840 FDA UDI
FDA Product Code
LZC FDA UDI
GMDN Term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial 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

No

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
MRI Safety
MR Safe FDA UDI

Category: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

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

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55d3ead1-929d-45be-941f-04bfd85f9f2b 33 fields · synced Jun 8, 2026