Finesse

GUDID 00850058725017

Black Nitrile powder free Exam Gloves Medium (case) 1/10/100

Direct Marketing USA LLC

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

• Primary Device ID: 00850058725017
• NIH Device Record Key: 119be714-d656-4dc1-aab7-6dd631af12f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finesse
• Version Model Number: DGN501
• Company DUNS: 079327950
• Company Name: Direct Marketing USA LLC
• Device Count: 1
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850058725017 [Package]; Contains: 00850058725055; Package: case [10 Units]; In Commercial Distribution
GS1	00850058725055 [Primary]

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: 2023-11-24
• Device Publish Date: 2023-11-16

On-Brand Devices [Finesse]

• 00850058725413: Black Nitrile powder Free Exam Gloves XX-Large (case) 1/10/100
• 00850058725017: Black Nitrile powder free Exam Gloves Medium (case) 1/10/100
• 00850058725079: Black Nitrile Powder free Exam Gloves X-Large (case) 1/10/100
• 00850058725062: Black Nitrile Powder free Exam Gloves Large (case) 1/10/100
• 00850058725048: Black Nitrile Powder Free Exam Gloves-Small (case) 1/10/100