FIRST STREET 72449-06770010

GUDID 00041512129797

72449 FIRST STREET EXAM GLOVE NITRILE LARGE BLUE

Smart & Final Stores LLC

Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 00041512129797
• NIH Device Record Key: 738e1498-08de-4790-bfe6-7ae7c173ee9f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FIRST STREET
• Version Model Number: 72449
• Catalog Number: 72449-06770010
• Company DUNS: 556948354
• Company Name: Smart & Final Stores LLC
• Device Count: 200
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Avoid Direct Sunlight, Keep Dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	00041512000003 [Unit of Use]
GS1	00041512129780 [Primary]
GS1	00041512129797 [Package]; Contains: 00041512129780; Package: CASE [4 Units]; In Commercial Distribution

FDA Product Code

• LZA: Polymer Patient Examination Glove

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-10
• Device Publish Date: 2026-03-02

On-Brand Devices [FIRST STREET]

• 00041512129810: 72453 FIRST STREET EXAM GLOVE NITRILE X-LARGE BLUE
• 00041512129797: 72449 FIRST STREET EXAM GLOVE NITRILE LARGE BLUE
• 00041512129773: 72448 FIRST STREET EXAM GLOVE NITRILE MEDIUM BLUE
• 00041512129759: 72450 FIRST STREET EXAM GLOVE NITRILE SMALL BLUE