| Primary Device ID | 00840682141635 |
| NIH Device Record Key | d11323ec-c586-46d4-bfbc-9b86d0683419 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CZT Upgrade |
| Version Model Number | H3906DE |
| Company DUNS | 532102365 |
| Company Name | G E MEDICAL SYSTEMS ISRAEL LTD. |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840682141635 [Primary] |
| KPS | System, tomography, computed, emission |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-05-15 |
| 00195278870490 - StarGuide MDD to MDR Upgrade | 2024-05-24 StarGuide SW and Labels Upgrade |
| 00195278755544 - StarGuide | 2024-04-26 StarGuide NM GANTRY MDR FINAL |
| 00195278794772 - D630 to D670 DR Upgrade | 2024-03-26 D630 to D670 DR NM GANTRY UPGRADE KIT |
| 00195278788252 - NM | 2023-11-23 830 NM GANTRY FINAL WITH NEW ROTOR - MDR CE |
| 00195278788269 - NMCT | 2023-11-22 870 DR NM GANTRY FINAL WITH NEW ROTOR - MDR CE |
| 00195278488619 - MyoSPECT | 2023-09-22 MyoSPECT MDR GANTRY |
| 00195278488626 - MyoSPECT ES | 2023-09-22 MyoSPECT ES MDR GANTRY |
| 00195278722546 - MyoSEPCT ES to MyoSPECT Upgrade | 2023-09-22 MyoSPECT ES to MyoSPECT Upgrade kit |