Neoss 91041

GUDID 06973993440099

Alliedstar Medical Equipment Co., Ltd.

Intraoral optical scanning system

• Primary Device ID: 06973993440099
• NIH Device Record Key: be13d304-c81c-4ba0-ba4a-f426fdc44591
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Neoss
• Version Model Number: NeoScan 2000-Handpiece
• Catalog Number: 91041
• Company DUNS: 703541803
• Company Name: Alliedstar Medical Equipment Co., Ltd.
• 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: false
• Lot Batch: false
• Serial Number: true
• 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	06973993440099 [Primary]

FDA Product Code

• NOF: System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations

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: 2023-09-12
• Device Publish Date: 2023-09-04

On-Brand Devices [Neoss]

• 06973993442086: Intraoral Scanner
• 06973993441263: NeoScan 2000-Charging Holder
• 06973993440099: NeoScan 2000-Handpiece