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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Anaesthesia face mask, single-use FDA UDI
Device Name
MASK FLEXIBLE CHILD SMALL ADULT SIZE 3 FDA UDI
Model / Reference
CHIMASK3 FDA UDI
Description
MASK FLEXIBLE CHILD SMALL ADULT SIZE 3 FDA UDI

Identifiers

Catalog Number
CHIMASK3 FDA UDI
Primary DI / UDI-DI
10885380191022 FDA UDI
FDA Product Code
BSJ FDA UDI
GMDN Term
Anaesthesia face mask, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5550 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Anaesthesia face mask, single-use

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia face mask, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c7a2b374-9afd-428a-b742-e1d93357377c 35 fields · synced Jun 8, 2026