| Primary Device ID | 04540217071630 |
| NIH Device Record Key | 0a1f7e47-643b-47c5-870c-82a5d7959dfb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SET-5002 |
| Version Model Number | 567-11700-12 |
| 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 | 04540217071630 [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 | 1 |
| Public Version Date | 2024-12-12 |
| Device Publish Date | 2024-12-04 |
| 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 |