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DermAssist® COATS™

FDA UDI

Class I (US FDA UDI)

by Innovative Healthcare Corporation

Identity

Trade Name
DermAssist® COATS™ FDA UDI
Generic Name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Gloves, Exam, Latex, Non-Sterile, Powder-Free, Colloidal Oatmeal, Therapeutic, XS FDA UDI
Model / Reference
124050 FDA UDI
Description
Gloves, Exam, Latex, Non-Sterile, Powder-Free, Colloidal Oatmeal, Therapeutic, XS FDA UDI

Identifiers

Primary DI / UDI-DI
20813172020578 FDA UDI
FDA Product Code
LYY FDA UDI
GMDN Term
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

DermAssist® COATS™ by Innovative Healthcare Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e7f0d5ae-8e29-41ac-bb0f-cb227e2eb1cc 33 fields · synced May 30, 2026