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FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Drive FDA UDI
Generic Name
Guayule-latex examination/treatment glove, non-powdered FDA UDI
Device Name
Personal CareAids to Daily Living Product Description: Sanitary Glove,12/PKG,6/CS FDA UDI
Model / Reference
146-RTL12086 FDA UDI
Description
Personal CareAids to Daily Living Product Description: Sanitary Glove,12/PKG,6/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00822383989808 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Guayule-latex examination/treatment glove, non-powdered 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Guayule-latex examination/treatment glove, non-powdered

Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 7e6e2c2c-bc0c-42c5-9983-0d2162f9a99b 33 fields · synced Jun 8, 2026