Primary Device ID | 04540217071616 |
NIH Device Record Key | bb6d015c-5186-49ed-a6c5-a014331cb6a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FDR Visionary Suite |
Version Model Number | 566-16130-83 |
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 | 04540217071616 [Primary] |
KPR | System, X-Ray, Stationary |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-03 |
Device Publish Date | 2024-05-24 |
04540217057450 | 566-16130-33 |
04540217057443 | 566-16130-32 |
04540217057436 | 566-16130-31 |
04540217052226 | 566-16130-23 |
04540217052219 | 566-16130-22 |
04540217052202 | 566-16130-21 |
04540217064724 | 566-16130-63 |
04540217064717 | 566-16130-62 |
04540217064700 | 566-16130-53 |
04540217064694 | 566-16130-52 |
04540217071616 | 566-16130-83 |
04540217071609 | 566-16130-82 |
04540217071593 | 566-16130-81 |
04540217071586 | 566-16130-80 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FDR VISIONARY SUITE 86312188 5191573 Live/Registered |
FUJIFILM Medical Systems U.S.A., Inc. 2014-06-17 |