SPI CONTACT

GUDID 07640156471748

Thommen Medical AG

Screw endosteal dental implant, two-piece

• Primary Device ID: 07640156471748
• NIH Device Record Key: 7ef084e7-f9c2-4449-9773-f1cf22d20b13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SPI CONTACT
• Version Model Number: 4.13.211
• 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: true
• 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	07640156471748 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072649

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

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 [SPI CONTACT ]

• 07640156471748: 4.13.211
• 07640156471731: 4.13.212
• 07640156471724: 4.13.213
• 07640156471717: 4.13.214
• 07640156471700: 4.13.220
• 07640156471694: 4.13.221
• 07640156471687: 4.13.222
• 07640156471670: 4.13.223
• 07640156471663: 4.13.224
• 07640156471656: 4.13.230
• 07640156471649: 4.13.231
• 07640156471632: 4.13.232
• 07640156471625: 4.13.233
• 07640156471618: 4.13.234
• 07640156471601: 4.13.240
• 07640156471595: 4.13.241
• 07640156471588: 4.13.242
• 07640156471571: 4.13.243
• 07640156471564: 4.13.244
• 07640156471557: 4.13.261
• 07640156471540: 4.13.262