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Remedy

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
REMEDY FDA UDI
Generic Name
Antimicrobial skin friction/moisture control fabric, single-patient reusable FDA UDI
Device Name
SHEET,DRIGO-HP,10X36 FDA UDI
Model / Reference
MSCWH219S FDA UDI
Description
SHEET,DRIGO-HP,10X36 FDA UDI

Identifiers

Catalog Number
MSCWH219S FDA UDI
Primary DI / UDI-DI
10193489009460 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Antimicrobial skin friction/moisture control fabric, single-patient reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

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: Antimicrobial skin friction/moisture control fabric, single-patient reusable

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

Similar devices

Also classified as Antimicrobial skin friction/moisture control fabric, single-patient reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI c7ebe56c-f1b7-46ae-a5f8-35b69445f611 36 fields · synced May 30, 2026