Dri-Aids

GUDID 20789594000675

YOUNG MICROBRUSH, LLC

Saliva absorbent

• Primary Device ID: 20789594000675
• NIH Device Record Key: da36378d-cc7b-4989-b9ff-d24f9635b7a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dri-Aids
• Version Model Number: 332190
• 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	00789594000671 [Primary]
GS1	10789594000678 [Package]; Contains: 00789594000671; Package: [750 Units]; In Commercial Distribution
GS1	20789594000675 [Package]; Contains: 10789594000678; 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