Ti DG1

GUDID 05057078000017

Titanium Powder Ti6-4-GD23

RENISHAW P L C

Dental casting non-noble alloy

• Primary Device ID: 05057078000017
• NIH Device Record Key: be6369f6-4857-42fd-bbea-fc4253206140
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ti DG1
• Version Model Number: UK2035
• Company DUNS: 217226935
• Company Name: RENISHAW P L C
• 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: true
• Serial Number: true
• 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	05057078000017 [Primary]
GS1	15057078000014 [Package]; Package: Carton [3 Units]; In Commercial Distribution

FDA Product Code

• EJH: Alloy, Metal, Base

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: 2018-04-20
• Device Publish Date: 2018-03-20

On-Brand Devices [Ti DG1]

• 05057078000031: Titanium Powder Ti6-4-GD23
• 05057078000017: Titanium Powder Ti6-4-GD23