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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
Anaesthesia face mask, single-use FDA UDI
Device Name
Anesthesia mask, Pediatric FDA UDI
Model / Reference
713-RG FDA UDI
Description
Anesthesia mask, Pediatric FDA UDI

Identifiers

Primary DI / UDI-DI
10612479274270 FDA UDI
510(k) Number
K953107 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia face mask, single-use

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

Similar devices

Also classified as Anaesthesia face mask, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1a92fe4c-9630-4844-8e43-5c442c5d40e5 34 fields · synced Jun 8, 2026