McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name: McKesson FDA UDI
Generic Name: Hypodermic needle, single-use FDA UDI
Device Name: Syringes with Safety Hypodermic Needles GLIDE|3cc 22G x 1 1/2 in FDA UDI
Model / Reference: 192-SN3C22105S FDA UDI
Description: Syringes with Safety Hypodermic Needles GLIDE|3cc 22G x 1 1/2 in FDA UDI

Identifiers

Primary DI / UDI-DI: 10612479248455 FDA UDI
FDA Product Code: FMF FDA UDI
FMI FDA UDI
GMDN Term: Hypodermic needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5860 FDA UDI
880.5570 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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Hypodermic needle, single-use General-purpose syringe, single-use Metered-delivery hypodermic syringe

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

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Also classified as Metered-delivery hypodermic syringe.

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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: Mckesson Medical-Surgical Inc.

Sources (1)

FDA UDI 81c285ff-ba7f-425f-90aa-354c69b15a60 33 fields · synced May 30, 2026