Primary Device ID | 04547410333527 |
NIH Device Record Key | a20af34b-1d6f-4bd2-865c-5bf0e193fd93 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DR-ID800CL |
Version Model Number | DR-ID800CL |
Company DUNS | 713565195 |
Company Name | FUJIFILM 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 | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx | |
Phone | +018002728465 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04547410333527 [Primary] |
LLZ | System, image processing, radiological |
MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2016-09-16 |
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