Publix UltiGuard

GUDID 30041415098788

Publix 4mm UltiGuard Safe Pack

PUBLIX SUPER MARKETS, INC.

Autoinjector needle

• Primary Device ID: 30041415098788
• NIH Device Record Key: e2118f5c-e020-4dda-8234-232ca0fb4e20
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Publix UltiGuard
• Version Model Number: 299819
• Company DUNS: 006922009
• Company Name: PUBLIX SUPER MARKETS, INC.
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00357515710031 [Unit of Use]
GS1	20041415098781 [Primary]
GS1	30041415098788 [Package]; Contains: 20041415098781; Package: UltiGuard [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K100812

FDA Product Code

• FMI: Needle, Hypodermic, Single Lumen

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-07-09
• Device Publish Date: 2024-07-01

On-Brand Devices [Publix UltiGuard]

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