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McKesson

FDA UDI

Class U (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Cold/cool therapy spray FDA UDI
Device Name
Topical Anesthetic Spray Mist FDA UDI
Model / Reference
140-MST FDA UDI
Description
Topical Anesthetic Spray Mist FDA UDI

Identifiers

Primary DI / UDI-DI
10612479220598 FDA UDI
FDA Product Code
MLY FDA UDI
GMDN Term
Cold/cool therapy spray FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cold/cool therapy spray

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

Similar devices

Also classified as Cold/cool therapy spray.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 096348ff-2b02-40b4-aa08-08491fe584f0 33 fields · synced May 30, 2026