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McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
Syringes with Safety Hypodermic Needles GLIDE|Thin wall/ Luer Lock 1cc 25G x 5/8 in (50/bx, 8/cs) FDA UDI
Model / Reference
306611 FDA UDI
Description
Syringes with Safety Hypodermic Needles GLIDE|Thin wall/ Luer Lock 1cc 25G x 5/8 in (50/bx, 8/cs) FDA UDI

Identifiers

Primary DI / UDI-DI
10612479262680 FDA UDI
FDA Product Code
FMI FDA UDI
FMF FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
880.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hypodermic needle, single-useGeneral-purpose syringe, single-use

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

Similar devices

Also classified as General-purpose syringe, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ee27980-da66-490c-8907-8d9c38bd8bb5 33 fields · synced Jun 1, 2026