Ultra Thin Lancets

GUDID 20041415032785

Publix Ultra Thin Lancets 28 Gauge lancets

PUBLIX SUPER MARKETS, INC.

Blood lancing device tip

• Primary Device ID: 20041415032785
• NIH Device Record Key: 337dff84-dad5-4895-81af-21ec0c64cf5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultra Thin Lancets
• Version Model Number: AT 0565PX
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Dimensions

• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge
• Needle Gauge: 28 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00041415032781 [Primary]
GS1	00384700565008 [Unit of Use]
GS1	20041415032785 [Package]; Contains: 00041415032781; Package: Case [200 Units]; In Commercial Distribution

FDA Product Code

• QRK: Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

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: 2023-07-03
• Device Publish Date: 2023-06-23

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