← Back to catalogue

Publix Insulin Syringe

FDA UDI

Class II (US FDA UDI)

by Publix Super Markets, Inc.

Identity

Trade Name
Publix Insulin Syringe FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
Publix 6mm 31G 3/10mL Insulin Syringe Box FDA UDI
Model / Reference
252353 FDA UDI
Description
Publix 6mm 31G 3/10mL Insulin Syringe Box FDA UDI

Identifiers

Primary DI / UDI-DI
10041415087788 FDA UDI
510(k) Number
K062702 FDA UDI
FDA Product Code
FMF FDA UDI
FMI FDA UDI
GMDN Term
Insulin syringe/needle, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
880.5570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

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: Insulin syringe/needle, basic

Publix Insulin Syringe by Publix Super Markets, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin syringe/needle, basic.

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 4b67958e-8d47-4e03-8a81-ef2a83c72162 34 fields · synced Jun 8, 2026