| Primary Device ID | 07640156475753 |
| NIH Device Record Key | 0cd1fd46-c73a-4301-836f-2444461882db |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SPI TEMPORARY |
| Version Model Number | 2.03.747 |
| 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 | 07640156475753 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07640156475753]
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 | 2015-10-24 |
| 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 |