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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
Multi-purpose therapeutic saline solution FDA UDI
Device Name
120 mL USP Sterile Saline, Foil Lid Container FDA UDI
Model / Reference
37-6220 FDA UDI
Description
120 mL USP Sterile Saline, Foil Lid Container FDA UDI

Identifiers

Primary DI / UDI-DI
40612479168556 FDA UDI
510(k) Number
K083042 FDA UDI
FDA Product Code
FRO FDA UDI
JOL FDA UDI
GMDN Term
Multi-purpose therapeutic saline solution FDA UDI

Classification

Device Class
U FDA UDI
Regulation Number
880.6740 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

Yes

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: Multi-purpose therapeutic saline solution

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

Similar devices

Also classified as Multi-purpose therapeutic saline solution.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bb4eabb5-cca8-49ad-a02d-382ec854e181 34 fields · synced May 30, 2026