ChemoPlus

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name: ChemoPlus FDA UDI
Generic Name: Non-respiratory device ambient air filter FDA UDI
Device Name: Vial Vent Chemo Dispensing Pin FDA UDI
Model / Reference: DP5201V FDA UDI
Description: Vial Vent Chemo Dispensing Pin FDA UDI

Identifiers

Catalog Number: DP5201V FDA UDI
Primary DI / UDI-DI: 20884527004222 FDA UDI
FDA Product Code: FMF FDA UDI
GMDN Term: Non-respiratory device ambient air filter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Non-respiratory device ambient air filter

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

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Also classified as Non-respiratory device ambient air filter.

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Coda® — LifeGlobal Group, LLC · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Cardinalhealth

Sources (1)

FDA UDI c0e9623d-f999-4d1d-95ec-a57dddaedfa7 36 fields · synced May 30, 2026