Dri-Aids

GUDID 10789594000692

YOUNG MICROBRUSH, LLC

Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent Saliva absorbent

• Primary Device ID: 10789594000692
• NIH Device Record Key: 9ac1e8a0-1e55-44d7-8af9-f5affe4c2bfd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dri-Aids
• Version Model Number: 332375
• Company DUNS: 929236305
• Company Name: YOUNG MICROBRUSH, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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	00789594000695 [Primary]
GS1	10789594000692 [Package]; Contains: 00789594000695; Package: [750 Units]; In Commercial Distribution
GS1	20789594000699 [Package]; Package: [13 Units]; In Commercial Distribution

FDA Product Code

• KHR: ABSORBER, SALIVA, PAPER

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: 2020-12-16
• Device Publish Date: 2020-12-08

On-Brand Devices [Dri-Aids]

• 10789594000692: 332375
• 20789594000682: 332325
• 20789594000675: 332190
• 20789594000668: 332125
• 20789594000651: 331375
• 20789594000644: 331320
• 20789594000637: 331190
• 20789594000620: 331125