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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Medical device cleaning/disinfection wipe FDA UDI
Device Name
WIPE,GERM,MICRO-KILL TWO,7X15,75CT FDA UDI
Model / Reference
MSC351281 FDA UDI
Description
WIPE,GERM,MICRO-KILL TWO,7X15,75CT FDA UDI

Identifiers

Catalog Number
MSC351281 FDA UDI
Primary DI / UDI-DI
10197344017690 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Medical device cleaning/disinfection wipe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical device cleaning/disinfection wipe

A comprehensive device for cleaning and disinfecting medical devices and equipment, using a moist pre-treated fabric to wipe surfaces. This single-use device is designed for general use in hospitals.

Similar devices

Also classified as Medical device cleaning/disinfection wipe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 390aa7aa-5b36-4a7a-ac4c-43455e5bf2a7 36 fields · synced Jul 21, 2026