Titanbasis for CAD/CAM

GUDID 07640156472417

Thommen Medical AG

Dental implant suprastructure kit

• Primary Device ID: 07640156472417
• NIH Device Record Key: 8a8fb0e7-8745-4606-9686-80b85c7877e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Titanbasis for CAD/CAM
• Version Model Number: 1.04.751
• Company DUNS: 481614829
• Company Name: Thommen Medical AG
• 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: 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	07640156472417 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102804

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[07640156472417]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-24

On-Brand Devices [Titanbasis for CAD/CAM]

• 07640156472424: 1.04.750
• 07640156472417: 1.04.751
• 07640156472400: 1.04.752
• 07640156472394: 1.04.753
• 07640156472387: 1.04.754
• 07640156472370: 1.04.760
• 07640156472363: 1.04.761
• 07640156472356: 1.04.762
• 07640156472349: 1.04.763
• 07640156472332: 1.04.764