| Primary Device ID | 07640156473858 | 
| NIH Device Record Key | bafa59b3-795a-445f-acf6-e41112a273cc | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | SPI TEMPORARY | 
| Version Model Number | 4.03.084 | 
| 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 Issuing Agency | Device ID | 
|---|---|
| GS1 | 07640156473858 [Primary] | 
| NHA | Abutment, Implant, Dental, Endosseous | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[07640156473858]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2018-12-07 | 
| Device Publish Date | 2015-09-24 | 
| 07640156475821 | 2.03.740 | 
| 07640156475814 | 2.03.741 | 
| 07640156475807 | 2.03.742 | 
| 07640156475791 | 2.03.743 | 
| 07640156475784 | 2.03.744 | 
| 07640156475777 | 2.03.745 | 
| 07640156475760 | 2.03.746 | 
| 07640156475753 | 2.03.747 | 
| 07640156475746 | 2.03.748 | 
| 07640156475739 | 2.03.749 | 
| 07640156474145 | 3.03.802 | 
| 07640156473896 | 4.03.080 | 
| 07640156473889 | 4.03.081 | 
| 07640156473872 | 4.03.082 | 
| 07640156473865 | 4.03.083 | 
| 07640156473858 | 4.03.084 | 
| 07640156473841 | 4.03.085 | 
| 07640156473834 | 4.03.086 | 
| 07640156473827 | 4.03.087 | 
| 07640156473810 | 4.03.088 | 
| 07640156473803 | 4.03.089 |