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MedSource Antiseptic Towelettes

FDA UDI

Class I (US FDA UDI)

by Medsource International Llc

Identity

Trade Name
MedSource Antiseptic Towelettes FDA UDI
Generic Name
Antiseptic skin towelette FDA UDI
Device Name
Alcohol Prep Pad, medium FDA UDI
Model / Reference
MS-17402 FDA UDI
Description
Alcohol Prep Pad, medium FDA UDI

Identifiers

Catalog Number
Not Applicable FDA UDI
Primary DI / UDI-DI
00816703025574 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Antiseptic skin towelette 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

Yes

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: Antiseptic skin towelette

MedSource Antiseptic Towelettes by Medsource International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antiseptic skin towelette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medsource International Llc

Sources (1)

  • FDA UDI 6cb12db2-6f2d-4997-a496-74f3f6fb1de1 34 fields · synced May 30, 2026