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ChemoPlus

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
ChemoPlus FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, sterile FDA UDI
Device Name
Chemotherapy Patient Examination Gloves 8 mil, Nitrile, Powder-free, X-Large FDA UDI
Model / Reference
CTS731XL FDA UDI
Description
Chemotherapy Patient Examination Gloves 8 mil, Nitrile, Powder-free, X-Large FDA UDI

Identifiers

Catalog Number
CTS731XL FDA UDI
Primary DI / UDI-DI
10884521132580 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Nitrile examination/treatment glove, non-powdered, sterile 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 29 Centimeter FDA UDI

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

ChemoPlus by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI d799a6d9-9db8-499e-b98f-64b44421ce52 37 fields · synced Jun 1, 2026