Publix UltiGuard

GUDID 30041415099785

Pubix 6mm UltiGuard Safe Pack

PUBLIX SUPER MARKETS, INC.

Autoinjector needle
Primary Device ID30041415099785
NIH Device Record Keya13b4932-38d2-4412-94be-ffdd622b26a2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePublix UltiGuard
Version Model Number299926
Company DUNS006922009
Company NamePUBLIX SUPER MARKETS, INC.
Device Count100
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100357515710147 [Unit of Use]
GS120041415099788 [Primary]
GS130041415099785 [Package]
Contains: 20041415099788
Package: UltiGuard [12 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FMINeedle, Hypodermic, Single Lumen

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-09
Device Publish Date2024-07-01

On-Brand Devices [Publix UltiGuard]

30041415099785Pubix 6mm UltiGuard Safe Pack
30041415098788Publix 4mm UltiGuard Safe Pack

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