| Primary Device ID | 00810035220119 | 
| NIH Device Record Key | 3c80c9d9-3044-4068-a6db-4f31dd2b04a5 | 
| 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 | 00810035220119 [Primary] | 
| IZL | System, X-Ray, Mobile | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[00810035220119]
Liquid Chemical
[00810035220119]
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 |