| Primary Device ID | 07640156471687 |
| NIH Device Record Key | c08d5228-d567-4711-8d44-1b9c4abb08f1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SPI CONTACT |
| Version Model Number | 4.13.222 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 07640156471687 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-24 |
| 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 |