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 |