ACRY CETTE 0130001

GUDID 18056865013012

DENTAL MANUFACTURING SPA

Resin artificial teeth

• Primary Device ID: 18056865013012
• NIH Device Record Key: d125bb16-60e2-4b37-82f0-e8a2a97cfd30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACRY CETTE
• Version Model Number: ACRY CETTE 6 UPPER
• Catalog Number: 0130001
• Company DUNS: 435782248
• Company Name: DENTAL MANUFACTURING SPA
• Device Count: 6
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056865013015 [Primary]
GS1	18056865013012 [Unit of Use]

FDA Product Code

• PZY: Additively Manufactured, Preformed, Resin Denture Tooth

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: 2020-02-19
• Device Publish Date: 2020-02-11

On-Brand Devices [ACRY CETTE ]

• 18056865013043: ACRY CETTE 8 LOWER
• 18056865013036: ACRY CETTE 8 UPPER
• 18056865013029: ACRY CETTE 6 LOWER
• 18056865013012: ACRY CETTE 6 UPPER