Primary Device ID | 00850229007102 |
NIH Device Record Key | 43fcd698-50b7-464f-b436-00d9a8ecf6ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | StatFax |
Version Model Number | 1904+ |
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 | 00850229007102 [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 |