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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
Saline Topical solution FDA UDI
Model / Reference
1723 FDA UDI
Description
Saline Topical solution FDA UDI

Identifiers

Primary DI / UDI-DI
20612479271283 FDA UDI
510(k) Number
K993969 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Multi-purpose therapeutic saline solution FDA UDI

Classification

Device Class
U 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: 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

K993969 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 7ccf4756-af02-4397-89fc-94918144789b 34 fields · synced Jun 8, 2026