ACRY ROCK V. 0010013

GUDID 18056865001132

DENTAL MANUFACTURING SPA

Resin artificial teeth

• Primary Device ID: 18056865001132
• NIH Device Record Key: a1d2900f-1f2b-41df-ba32-7d08ab8c2f37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACRY ROCK V.
• Version Model Number: ACRY ROCK V. 6 UPPER
• Catalog Number: 0010013
• 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	08056865001135 [Primary]
GS1	18056865001132 [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: 2020-03-06
• Device Publish Date: 2020-02-27

On-Brand Devices [ACRY ROCK V. ]

• 18056865001163: ACRY ROCK V. 8 LOWER
• 18056865001156: ACRY ROCK V. 8 UPPER
• 18056865001149: ACRY ROCK V. 6 LOWER
• 18056865001132: ACRY ROCK V. 6 UPPER