Primary Device ID | 00357599000257 |
NIH Device Record Key | adb5f9d2-e1f6-4e2a-821c-f8456d4a53d7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Precision Xceed Pro |
Version Model Number | 70907-05 |
Catalog Number | 70907-05 |
Company DUNS | 966390890 |
Company Name | ABBOTT DIABETES CARE INC |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | true |
Phone | +1(877)529-7185 |
xx@xx.xx |
Storage Environment Temperature | Between -4 Degrees Fahrenheit and 122 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00357599000257 [Primary] |
JIN | NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2016-08-26 |
00357599000257 | Precision Xceed Pro |
00357599000189 | Precision Xceed Pro Blood Glucose and ß-Ketone Monitoring System |
00357599000158 | Precision Xceed Pro Blood Glucose and ß-Ketone Monitoring System |
00357599000134 | Precision Xceed Pro Blood Glucose and ß-Ketone Monitoring System |
35021791709350 | Precision Xceed Pro Blood ß-Ketone Test Strips |
30093815709320 | Precision Xceed Pro Blood Glucose Test Strips |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRECISION XCEED PRO 77225761 3437436 Live/Registered |
Abbott Laboratories 2007-07-10 |