Primary Device ID | 05055273201734 |
NIH Device Record Key | 02c4f824-1fbf-4bec-8950-19fd3a29daee |
Commercial Distribution Discontinuation | 2016-09-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | CRP |
Version Model Number | CP2572 |
Catalog Number | CP2572 |
Company DUNS | 227530649 |
Company Name | RANDOX LABORATORIES LIMITED |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
05055273201833 | The CRP test system is intended for the quantitative in vitro determination of CRP concentration |
05055273201826 | The CRP test system is intended for the quantitative in vitro determination of CRP concentration |
05055273201819 | The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Prot |
05055273201765 | The CRP test system is intended for the quantitative in vitro determination of CRP concentration |
05055273201758 | The XCRP method used on the Dimension clinical chemistry system is an in vitro diagnostic test i |
05055273201741 | The device is a latex agglutination slide test intended for qualitative and semi-quantitative in |
05055273201734 | The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Prot |
05055273201642 | The device is a latex agglutination slide test intended for qualitative and semi-quantitative in |