| Primary Device ID | 04540217040926 | 
| NIH Device Record Key | 58850145-5dee-44f1-b274-f87d7521278b | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | SONIALVISION G4 | 
| Version Model Number | 503-78000-23 | 
| 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 | true | 
| 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 | 04540217040926 [Primary] | 
| JAA | System, X-Ray, Fluoroscopic, Image-Intensified | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2018-10-29 | 
| Device Publish Date | 2018-09-28 | 
| 04540217040964 | 503-78000-27 | 
| 04540217040957 | 503-78000-26 | 
| 04540217040926 | 503-78000-23 | 
| 04540217064816 | 503-78000-54 | 
| 04540217064809 | 503-78000-24 | 
| 04540217041060 | 566-10000-47 | 
| 04540217041053 | 566-10000-46 | 
| 04540217041046 | 566-10000-43 | 
| 04540217041039 | 566-10000-42 | 
| 04540217041022 | 566-10000-41 | 
| 04540217040896 | 503-78000-53 | 
| 04540217040889 | 503-78000-52 | 
| 04540217040872 | 503-78000-51 |