Purpose Select

GUDID 10850050195112

Purpose Veterinary Supply 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: 10850050195112
• NIH Device Record Key: fd904c0a-39f4-4c8d-9998-7324cf9bde1c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Purpose Select
• Version Model Number: XS-BLK-300
• Company DUNS: 118923926
• Company Name: Purpose Veterinary Supply LLC
• Device Count: 300
• 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	00850050195115 [Primary]
GS1	10850050195112 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K001619

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: 2023-05-09
• Device Publish Date: 2023-05-01

On-Brand Devices [Purpose Select ]

• 10850050195150: XL-BLK-250
• 10850050195143: L-BLK-300
• 10850050195136: M-BLK-300
• 10850050195129: S-BLK-3.00
• 10850050195112: XS-BLK-300
• 10850050195105: XL-BLU-250
• 10850050195099: L-BLU-300
• 10850050195082: M-BLU-300
• 10850050195075: S-BLU-300
• 10850050195068: XS-BLU-300
• 10850050195051: XL-BLU-100
• 10850050195044: L-BLU-100
• 10850050195037: M-BLU-100
• 10850050195020: S-BLU-100
• 10850050195013: XS-BLU-100