| Primary Device ID | 00850229007010 |
| NIH Device Record Key | d4b705e9-ac89-4eb7-8c4c-5c14e65d3bc2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | StatFax |
| Version Model Number | 4700 |
| 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 | 00850229007010 [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 |