Primary Device ID | 04540217041060 |
NIH Device Record Key | 897d567d-1068-49d3-a6cd-5174e945adf7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SONIALVISION G4 |
Version Model Number | 566-10000-47 |
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 | 04540217041060 [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 | 2 |
Public Version Date | 2025-05-28 |
Device Publish Date | 2019-08-14 |
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 |