| Primary Device ID | 04540217060825 | 
| NIH Device Record Key | 8bc3b153-0aed-45e3-8bf2-fdbb1a2255e6 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | 0.4/0.7JG326 D-265 | 
| Version Model Number | 582-24838-11 | 
| Company DUNS | 690558747 | 
| Company Name | SHIMADZU CORPORATION | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| 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 | 04540217060825 [Primary] | 
| ITY | Assembly, Tube Housing, X-Ray, Diagnostic | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2025-05-28 | 
| Device Publish Date | 2019-07-23 | 
| 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 |