← Back to catalogue

Publix

FDA UDI

Class I (US FDA UDI)

by Publix Super Markets, Inc.

Identity

Trade Name
Publix FDA UDI
Generic Name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
PUB LATEX MED EXAM GLOVES FDA UDI
Model / Reference
121307 FDA UDI
Description
PUB LATEX MED EXAM GLOVES FDA UDI

Identifiers

Catalog Number
121307 FDA UDI
Primary DI / UDI-DI
00041415028746 FDA UDI
510(k) Number
K051404 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Publix by Publix Super Markets, Inc. — 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.

Cleared under the same submission

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

Sources (1)

  • FDA UDI 405df3dc-5cf8-427b-8405-cb01bd6fc69d 35 fields · synced May 30, 2026