SAFEHAND M2650026

GUDID 40727351800902

SH GLOVE POWDER FREE EXAM NITRILE MEDIUM BLACK

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

• Primary Device ID: 40727351800902
• NIH Device Record Key: a389d965-e787-494e-807d-f653781f8992
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SAFEHAND
• Version Model Number: M2650026
• Catalog Number: M2650026
• 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	00727351800904 [Unit of Use]
GS1	20727351800908 [Primary]
GS1	40727351800902 [Package]; Contains: 20727351800908; 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: 2024-04-22
• Device Publish Date: 2024-04-12

On-Brand Devices [SAFEHAND]

• 40727351800896: SH GLOVE POWDER FREE EXAM NITRILE SMALL BLACK
• 40727351800926: SH GLOVE POWDER FREE EXAM NITRILE X-LARGE BLACK
• 40727351800919: SH GLOVE POWDER FREE EXAM NITRILE LARGE BLACK
• 40727351800902: SH GLOVE POWDER FREE EXAM NITRILE MEDIUM BLACK
• 40727351800964: SH GLOVE POWDER FREE EXAM NITRILE X-LARGE BLUE
• 40727351800957: SH GLOVE POWDER FREE EXAM NITRILE LARGE BLUE
• 00727351800942: SH GLOVE POWDER FREE EXAM NITRILE MEDIUM BLUE
• 40727351800933: SH GLOVE POWDER FREE EXAM NITRILE SMALL BLUE