Avalon Biomed NeoSolv

GUDID 00810118106422

Avalon Biomed NeoSolv - 8 oz Bottle

NUSMILE, LTD.

Root canal cleaning solution

• Primary Device ID: 00810118106422
• NIH Device Record Key: 73270115-e210-4ab0-9f5d-4cde94ee4e1d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Avalon Biomed NeoSolv
• Version Model Number: ABNS8
• Company DUNS: 185497372
• Company Name: NUSMILE, LTD.
• Device Count: 1
• 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: false
• Expiration Date: true
• 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	00810118106422 [Primary]

FDA Product Code

• KJJ: Cleanser, Root Canal

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: 2025-03-27
• Device Publish Date: 2025-03-19

On-Brand Devices [Avalon Biomed NeoSolv]

• 00810118106422: Avalon Biomed NeoSolv - 8 oz Bottle
• 00810118106415: Avalon Biomed NeoSolv - 4 oz Bottle