Relion ULTRA-THIN Lancets

GUDID 05078742026485

WAL-MART STORES, INC.

Blood lancet, single-use

• Primary Device ID: 05078742026485
• NIH Device Record Key: 3a7033f6-dff6-4c71-ae9f-0c90acb9d481
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Relion ULTRA-THIN Lancets
• Version Model Number: 01-0133
• Company DUNS: 051957769
• Company Name: WAL-MART STORES, INC.
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00078742026480 [Primary]
GS1	05078742026485 [Unit of Use]

FDA Product Code

• FMK: Single Use Only Blood Lancet With 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: 2022-09-07
• Device Publish Date: 2022-08-30

On-Brand Devices [Relion ULTRA-THIN Lancets]

• 05681131098859: 01-0130
• 05681131060412: 01-0126
• 05078742026485: 01-0133
• 00078742026442: 01-0130