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ChemoPlus

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
ChemoPlus FDA UDI
Generic Name
Infectious waste absorbent FDA UDI
Device Name
Prep Mat FDA UDI
Model / Reference
CT0303-1 FDA UDI
Description
Prep Mat FDA UDI

Identifiers

Catalog Number
CT0303-1 FDA UDI
Primary DI / UDI-DI
20884527004383 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Infectious waste absorbent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 69 Inch FDA UDI
Width — 16 Inch FDA UDI

Category: Infectious waste absorbent

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

Similar devices

Also classified as Infectious waste absorbent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI e9cd556d-13d6-4f11-a5d7-22a32ebc6842 37 fields · synced Jun 1, 2026