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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
Intravenous insulin syringe FDA UDI
Device Name
Insulin Syringe with Needle 1cc 29G x 1/2" FDA UDI
Model / Reference
16-SN1C2905 FDA UDI
Description
Insulin Syringe with Needle 1cc 29G x 1/2" FDA UDI

Identifiers

Primary DI / UDI-DI
20612479231690 FDA UDI
510(k) Number
K151949 FDA UDI
K993017 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Intravenous insulin syringe 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: Intravenous insulin syringe

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

Similar devices

Also classified as Intravenous insulin syringe.

Cleared under the same submission

K151949 also covers:

K993017 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI 124d06bd-1cc0-4798-901a-90d78f1f37d9 34 fields · synced Jun 1, 2026