| Primary Device ID | 07640156473681 |
| NIH Device Record Key | d6982739-049b-4633-89cf-cb2b49b8a09e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SPI RETAIN |
| Version Model Number | 4.03.506 |
| 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 | 07640156473681 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07640156473681]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2015-09-24 |
| 07640156473964 | 4.03.040 |
| 07640156473957 | 4.03.041 |
| 07640156473940 | 4.03.042 |
| 07640156473933 | 4.03.043 |
| 07640156473926 | 4.03.048 |
| 07640156473919 | 4.03.049 |
| 07640156473902 | 4.03.070 |
| 07640156473797 | 4.03.380 |
| 07640156473780 | 4.03.381 |
| 07640156473773 | 4.03.382 |
| 07640156473766 | 4.03.388 |
| 07640156473759 | 4.03.420 |
| 07640156473742 | 4.03.421 |
| 07640156473735 | 4.03.422 |
| 07640156473728 | 4.03.423 |
| 07640156473711 | 4.03.428 |
| 07640156473704 | 4.03.500 |
| 07640156473698 | 4.03.502 |
| 07640156473681 | 4.03.506 |
| 07640156473674 | 4.03.507 |
| 07640156471830 | 4.03.501 |