← Back to catalogue

First Line

FDA UDI

Class I (US FDA UDI)

by Solace Trading LLC

Identity

Trade Name
FIRST LINE FDA UDI
Generic Name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Model / Reference
LATEX GLOVES - EXTRA-LARGE - CL8060L - 100 PCS FDA UDI

Identifiers

Primary DI / UDI-DI
00860007772375 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-antimicrobialGuayule-latex examination/treatment glove, non-powdered

First Line by Solace Trading LLC — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Solace Trading LLC

Sources (1)

  • FDA UDI 9e375d07-09cc-4a59-ac53-6aad4153f9e8 32 fields · synced May 30, 2026