ARIA 89363

GUDID 00816594020535

ARIA,INCISAL,RFL,5GM

DANVILLE MATERIALS, LLC

Light-cured dental restorative composite resin

• Primary Device ID: 00816594020535
• NIH Device Record Key: ee499cd6-1b2d-4d8b-8b20-7d12ae518df7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ARIA
• Version Model Number: 89363
• Catalog Number: 89363
• Company DUNS: 601302743
• Company Name: DANVILLE MATERIALS, LLC
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(760)743-7744
• Email: xxx@xxx.xxx
• Phone: +1(760)743-7744
• Email: xxx@xxx.xxx
• Phone: +1(760)743-7744
• Email: xxx@xxx.xxx

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 and 74 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816594020535 [Primary]

FDA Product Code

• EBF: MATERIAL, TOOTH SHADE, RESIN

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-22

On-Brand Devices [ARIA]

• 00816594020542: ARIA,INTRO KIT 4 X 1GM
• 00816594020535: ARIA,INCISAL,RFL,5GM
• 00816594020528: ARIA,INCISAL,RFL,1GM
• 00816594020511: ARIA,A3.5,RFL,5GM
• 00816594020504: ARIA,A3.5,1GM
• 00816594020498: ARIA,A2,RFL,5GM
• 00816594020481: ARIA,A2,RFL,1GM,FA
• 00816594020474: ARIA,A1,RFL,5GM
• 00816594020436: ARIA,A1,RFL,1GM,FA