GP Comprehensive QC Set

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Details

GP Comprehensive QC Set contains two KWIK-STIKs of each strain listed below (18 KWIK-STIKs total).

0761PEnterococcus casseliflavus derived from ATCC® 700327™*
0223PEnterococcus saccharolyticus derived from ATCC® 43076™*
0126PKocuria kristinae derived from ATCC® BAA-752™*
0130PListeria monocytogenes derived from ATCC® BAA-751™*
0134PStaphylococcus saprophyticus derived from ATCC® BAA-750™*
0764PStaphylococcus sciuri subsp. sciuri derived from ATCC® 29061™*
0101PStreptococcus equi subsp. zooepidemicus derived from ATCC® 43079™*
0947PStreptococcus pneumoniae derived from ATCC® 49619™*
0136PStreptococcus thermophilus derived from ATCC® 19258™*

General Information

Documentation

Product FormatQC Sets and Panels: KWIK-STIK™ 2 Pack

Strain Characteristics0764P Mammaliicoccus sciuri derived from ATCC® 29061™* requires a VS 16-6 or 16-6a permit from USDA.

ATCC® 19258™* formerly Streptococcus thermophilus

Test MethodMicrobial Identification

Catalog number5193

Industry TypeClinical, Medical Devices, Research

DisclaimerAs Microbiologics transitions to the EU In Vitro Diagnostic Regulation (IVDR), there will be a period of time that we will be shipping existing inventory labeled under the IVDD and new product labeled under the IVDR. These products are identical but are labeled slightly differently due to the changes in EU regulation. It is important to obtain the correct IFU for your product. For products that are labeled as CE Marked under the IVDR, the CE Mark symbol on the actual product labeling DOES include a four digit number beside it. Please use the IFU labeled “IVDR Instructions for Use: LYFO DISK and KWIK-STIK”.

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Documentation

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Catalog No. 5193P Name Change Letter

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Documentation

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Instructions for Use

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