| Primary Device ID | 00850229007034 | 
| NIH Device Record Key | 93b8be95-b5fa-479f-b0d6-90969e31223c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | StatFax | 
| Version Model Number | 4200 | 
| Company DUNS | 071065130 | 
| Company Name | AWARENESS TECHNOLOGY, INCORPORATED | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| 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 | 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 | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00850229007034 [Primary] | 
| JJQ | Colorimeter, Photometer, Spectrophotometer For Clinical Use | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2023-06-13 | 
| Device Publish Date | 2023-06-05 | 
| 00850229007102 | 1904+ | 
| 00850229007089 | Digital Dry Bath | 
| 00850229007072 | Digital Dry Bath | 
| 00850229007041 | 3300 | 
| 00850229007034 | 4200 | 
| 00850229007027 | 4500 | 
| 00850229007010 | 4700 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  STATFAX  75113540  not registered Dead/Abandoned | STATFAX, INC. 1996-06-04 |