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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Non-rebreathing oxygen face mask FDA UDI
Device Name
Aerosol Mask Pediatric VENTED | MULTIDIRECTIONAL SWIVEL | SINGLE PATIENT USE FDA UDI
Model / Reference
32632 FDA UDI
Description
Aerosol Mask Pediatric VENTED | MULTIDIRECTIONAL SWIVEL | SINGLE PATIENT USE FDA UDI

Identifiers

Primary DI / UDI-DI
20612479208241 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Non-rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

Category: Non-rebreathing oxygen face mask

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rebreathing oxygen face mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5052e11c-0273-4c62-8f9d-7e48dba3da96 33 fields · synced May 30, 2026