| Primary Device ID | 04540217032037 |
| NIH Device Record Key | 70514e6c-1cf2-420a-8c27-7e4b3c3c11e9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IA-12LT/HS |
| Version Model Number | 532-16886-01 |
| Company DUNS | 690558747 |
| Company Name | SHIMADZU CORPORATION |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04540217032037 [Primary] |
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-16 |
| 04540217040872 - SONIALVISION G4 | 2025-05-28 |
| 04540217040889 - SONIALVISION G4 | 2025-05-28 |
| 04540217040896 - SONIALVISION G4 | 2025-05-28 |
| 04540217041022 - SONIALVISION G4 | 2025-05-28 |
| 04540217041039 - SONIALVISION G4 | 2025-05-28 |
| 04540217041046 - SONIALVISION G4 | 2025-05-28 |
| 04540217041053 - SONIALVISION G4 | 2025-05-28 |
| 04540217041060 - SONIALVISION G4 | 2025-05-28 |