ADVANCE IF 51CF

GUDID 00810120951225

Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, SMALL

Diamond Gloves

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: 00810120951225
• NIH Device Record Key: 2dc5e51e-3ec6-4890-96ce-b6323795876d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ADVANCE IF 51CF
• Version Model Number: NCF-51S
• Company DUNS: 052262122
• Company Name: Diamond Gloves
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810120951201 [Unit of Use]
GS1	00810120951218 [Primary]
GS1	00810120951225 [Package]; Contains: 00810120951218; 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: 2023-06-30
• Device Publish Date: 2023-06-22

On-Brand Devices [ADVANCE IF 51CF]

• 00810120951348: Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, XX-LARGE
• 00810120951317: Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, X-LARGE
• 00810120951287: Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, LARGE
• 00810120951256: Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, MEDIUM
• 00810120951225: Powder Free Black Nitrile Examination Gloves, Chemo Tested & Fentanyl Protection, SMALL