Uniseal High-Risk Latex

GUDID 30744514001580

Latex Powder Free Textured Dark Blue Exam Gloves, Non-Sterile, Size L

Uniseal

Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 30744514001580
• NIH Device Record Key: 68ce0d0a-d8d4-4a51-a8cb-9cf66331e267
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Uniseal High-Risk Latex
• Version Model Number: 015-8
• Company DUNS: 782209340
• Company Name: Uniseal
• Device Count: 50
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	10744514001586 [Unit of Use]
GS1	20744514001583 [Primary]
GS1	30744514001580 [Package]; Contains: 20744514001583; Package: CASE [10 Units]; In Commercial Distribution

FDA Product Code

• LYY: Latex 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: 2022-08-30
• Device Publish Date: 2022-08-22

On-Brand Devices [Uniseal High-Risk Latex]

• 30744514001597: Latex Powder Free Textured Dark Blue Exam Gloves, Non-Sterile, Size XL
• 30744514001580: Latex Powder Free Textured Dark Blue Exam Gloves, Non-Sterile, Size L
• 30744514001573: Latex Powder Free Textured Dark Blue Exam Gloves, Non-Sterile, Size M
• 30744514001566: Latex Powder Free Textured Dark Blue Exam Gloves, Non-Sterile, Size S
• 30744514001504: Latex Powder Free Textured Dark Blue Exam Gloves, Non-Sterile, Size XXL