Clinical Chemistry

B35181359 | CK ISOCONTROL SERUM

Description
Human controlserum used as a quality control reagent to test Accuracy and precision of CK diagnostic methods. The Control can be used manually through the use of spectrophotometer or photometer...
Method: 
Content: 2 x 5 ml

IFU: OK | MSDS: NA

B35181700 | NORMAL CONTROL SERUM

Description
Normal human serum used as a quality control reagent to test Accuracy and precision of quantitative clinical chemistry diagnostic methods. The Control can be used manually through the use of...
Method: 
Content: 5 x 5 ml
IFU: OK | MSDS: NA

B35181701 | CLINICONTROL AB PATHOLOGICAL

Description
Abnormal serum used as a quality control reagent to test Accuracy and precision of quantitative clinical chemistry diagnostic methods. The Control can be used manually through the use of spectrophotometer...
Method: 
Content: 5 x 5 ml
IFU: OK | MSDS: NA

B35181702 | SUBSTRATE/ENZYME CALIBRATOR

Description
Human serum to be used for the calibration of quantitative immunochemical diagnostic methods. The Calibrator can be used manually through the use of spectrophotometer or photometer or with all automatic...
Method: 
Content: 5 x 3 ml
IFU: OK | MSDS: NA

B35182590 | CALIBRATOR HDL / LDL

Description
Human serum to be used for the calibration ofHDL/lDL cholesterol reagents with manual method or withautomatic methods. The reagent is obtained from defibrinated, freeze-dried human plasma.
Method: 
Content: 5 x 1 ml
IFU: OK | MSDS: NA

B35182597 | CONTROL HDL / LDL

Description
Human serum to be used as control of accuracy and precision forHDL/lDL cholesterol reagents, with manual method or withautomatic methods. The reagent is obtained from defibrinated, freeze-dried human plasma.
Method: 
Content: 5 x 3 ml
IFU: OK | MSDS: NA

B35282591 | TOTAL URINARY PROTEIN CALIBRATOR

Description
Device to be used for calibration purposes in the quantitative determination urinaryproteins in human urine in association withspecific applications procedures established by AlmaMedix Diagnostics International. The reagent can be used...
Method: 
Content: 3 x 1 ml
IFU: OK | MSDS: NA
 

B35282592 | LOW/HIGH CONTROL OF TOTAL URINARY PROTEIN

Description
Device to be used for Quality Control purposes to test Accuracy and precision of Urinary proteins diagnostic methods. The Control can be used manually through the use of spectrophotometer or...
Method: 
Content: 2 (3×1 ml)
IFU: OK | MSDS: NA

B75182500 | DIRECT BILIRUBIN

Description
Product for use in the quantitative determination in vitro of the concentration of Inorganic Phosphorusin human serum or urine. The reagent can be used manually through the use of spectrophotometer...
Method: Method UV End-Point.
Content: 12 x 20ml
IFU: OK | MSDS: OK

B75182510 | MAGNESIUM

Description
Product for use in the quantitative determination in vitro of the concentration of Magnesiumin human serum, plasma or urine. The reagent can be used manually through the use of spectrophotometer...
Method: Method Xylidyl-blue.
Content: 12 x 20 ml
IFU: OK | MSDS: OK

B75182511 | MAGNESIUM

Description
Product for use in the quantitative determination in vitro of the concentration of Magnesiumin human serum, plasma or urine. The reagent can be used manually through the use of spectrophotometer...
Method: Method Xylidyl-blue.
Content: 8 x 10 ml
IFU: OK | MSDS: OK

B75182512 | TOTAL PROTEIN

Description
Product for use in the quantitative determination in vitro of the concentration of Total Proteinsin human serum or plasma. The reagent can be used manually through the use of spectrophotometer...
Method: Method Biuret.
Content: 10 x 60 ml
IFU: OK | MSDS: OK