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Medline

FDA UDI

Class U (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Non-antimicrobial wound irrigation solution, saline FDA UDI
Device Name
CLEANSER, WOUND, PUREWASH, 4OZ, POUR FDA UDI
Model / Reference
MSC9004 FDA UDI
Description
CLEANSER, WOUND, PUREWASH, 4OZ, POUR FDA UDI

Identifiers

Catalog Number
MSC9004 FDA UDI
Primary DI / UDI-DI
10197344139873 FDA UDI
510(k) Number
K233399 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Non-antimicrobial wound irrigation solution, saline FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

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: Non-antimicrobial wound irrigation solution, saline

Medline by Medline Industries, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-antimicrobial wound irrigation solution, saline.

Cleared under the same submission

K233399 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eaa2d386-9c2b-43b8-b1ac-9e0e7c3ac53f 37 fields · synced May 30, 2026