PRIMESOURCE 21000000

GUDID 00727351804780

P/S Nitrile Exam P/F BLK SML

Bunzl USA Holdings 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

• Primary Device ID: 00727351804780
• NIH Device Record Key: 276ac86b-ece5-4094-86a2-39f38e0e9dc6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRIMESOURCE
• Version Model Number: 21000000
• Catalog Number: 21000000
• Company DUNS: 799540588
• Company Name: Bunzl USA Holdings LLC
• Device Count: 100
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00727351804780 [Primary]
GS1	20727351804784 [Unit of Use]
GS1	40727351804788 [Package]; Package: CASE [10 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: 2024-05-31
• Device Publish Date: 2024-05-23

On-Brand Devices [PRIMESOURCE]

• 40727351064571: P/S VNYL MEDICAL EXAM POWDER FREE X-LRG CLEAR
• 40727351064472: P/S VNYL MEDICAL EXAM POWDER FREE LARGE CLEAR
• 00727351064375: P/S VNYL MEDICAL EXAM POWDER FREE MED CLEAR
• 40727351064274: P/S VNYL MEDICAL EXAM POWDER FREE SMALL CLEAR
• 00727351804858: P/S Nitrile Exam P/F BLUE XL
• 00727351804841: P/S Nitrile Exam P/F BLUE LRG
• 00727351804834: P/S Nitrile Exam P/F BLUE MED
• 00727351804827: P/S Nitrile Exam P/F BLUE SML
• 00727351804810: P/S Nitrile Exam P/F BLK XL
• 00727351804803: P/S Nitrile Exam P/F BLK LRG
• 00727351804797: P/S Nitrile Exam P/F BLK MED
• 00727351804780: P/S Nitrile Exam P/F BLK SML