Primary Device ID | 04540217020225 |
NIH Device Record Key | a9fe345d-6a3e-445f-b25a-362bb6a30d6c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IA-16LD/HS |
Version Model Number | 532-16728-01 |
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 | 04540217020225 [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 | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
04540217071630 - SET-5002 | 2024-12-12 |
04540217071586 - FDR Visionary Suite | 2024-06-03 |
04540217071593 - FDR Visionary Suite | 2024-06-03 |
04540217071609 - FDR Visionary Suite | 2024-06-03 |
04540217071616 - FDR Visionary Suite | 2024-06-03 |
04540217071319 - RADspeed Pro | 2024-04-09 |
04540217071326 - RADspeed Pro | 2024-04-09 |
04540217071333 - RADspeed Pro | 2024-04-09 |