Better Touch

GUDID 00815947007537

CENTRAL ASSOCIATION FOR THE BLIND, INC.

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: 00815947007537
• NIH Device Record Key: 4581d365-b2c2-40fe-a119-4e70ea3f45c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Better Touch
• Version Model Number: 809.5
• Company DUNS: 099903148
• Company Name: CENTRAL ASSOCIATION FOR THE BLIND, INC.
• Device Count: 50
• 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: false
• Serial Number: false
• Manufacturing Date: false
• 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	00810007942872 [Unit of Use]
GS1	00815947007537 [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: 2023-04-06
• Device Publish Date: 2023-03-29

On-Brand Devices [Better Touch ]

• 00815947007810: 807.5HHC
• 00815947007803: 807.4HHC
• 00815947007797: 807.3HHC
• 00815947007780: 807.2HHC
• 00815947007551: 809.7
• 00815947007544: 809.6
• 00815947007537: 809.5
• 00815947007520: 809.4
• 00815947007513: 809.3
• 00815947007506: 809.2
• 00815947007490: 809.1
• 00815947006905: 807.1
• 00815947004550: 807.6
• 00815947004505: 802.1
• 00815947004499: 825.6
• 00815947004482: 825.5
• 00815947004475: 825.4
• 00815947004468: 825.3
• 00815947004451: 825.2
• 00815947004406: 802.4
• 00815947004390: 802.3
• 00815947004383: 802.2
• 00815947004376: 802.5
• 00815947004369: 804.5
• 00815947004352: 804.4
• 00815947004345: 804.3
• 00815947004338: 804.2
• 00815947004321: 807.5
• 00815947004314: 807.4
• 00815947004307: 807.3
• 00815947004291: 807.2
• 00810007941325: 880.1
• 00810007941318: 880.6
• 00810007941301: 880.5
• 00810007941295: 880.4
• 00810007941288: 880.3
• 00810007941271: 880.2