Primary Device ID | 00810035220256 |
NIH Device Record Key | 802fc9d7-8419-46b6-81e5-c34e4b0567fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AcuityPDR |
Version Model Number | Standard |
Company DUNS | 005057263 |
Company Name | RADMEDIX, LLC |
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 | 00810035220256 [Primary] |
IZL | System, X-Ray, Mobile |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810035220256]
Liquid Chemical
[00810035220256]
Liquid Chemical
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-12 |
Device Publish Date | 2020-05-04 |
00810035220300 | Standard |
00810035220294 | Standard |
00810035220287 | Standard |
00810035220270 | Standard |
00810035220263 | Standard |
00810035220256 | Standard |
00810035220249 | Standard |
00810035220232 | Standard |
00810035220225 | Standard |
00810035220218 | Standard |
00810035220201 | Standard |
00810035220195 | Standard |
00810035220188 | Standard |
00810035220171 | Standard |
00810035220164 | Standard |
00810035220157 | Standard |
00810035220140 | Standard |
00810035220133 | Standard |
00810035220126 | Standard |
00810035220119 | Standard |
00810035220362 | Standard |
00810035220355 | Standard |
00810035220348 | Standard |
00810035220331 | Standard |