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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
Insulin syringe/needle, safety FDA UDI
Device Name
Syringes with Safety Needles 3/10CC | INSULIN 31G x 5/16 in (100/bx, 8/cs) FDA UDI
Model / Reference
16-SFTYSFN7 FDA UDI
Description
Syringes with Safety Needles 3/10CC | INSULIN 31G x 5/16 in (100/bx, 8/cs) FDA UDI

Identifiers

Primary DI / UDI-DI
20612479228591 FDA UDI
FDA Product Code
MEG FDA UDI
GMDN Term
Insulin syringe/needle, safety FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Insulin syringe/needle, safety

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

Similar devices

Also classified as Insulin syringe/needle, safety.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c2489a98-1380-4160-969b-8592bab3f487 33 fields · synced May 31, 2026