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QC Sets and Panels: Helix Elite™
Catalog No. 8254

Blood Culture Identification Control Panel (43 Targets)

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Details

Details

Blood Culture Identification Control Panel (43 Targets) contains six inactivated pre-pooled positive control 1 pellets, six inactivated pre-pooled positive control 2 pellets, and 6 inactivated negative control pellets (18 vials/pellets total). The negative control pellets are blank and do not contain microorganisms.

BCID2 Positive Control 1 (six vials/pellets):

  • Bacteroides fragilis
  • Klebsiella aerogenes
  • Salmonella Typhimurium
  • Stenotrophomonas maltophilia
  • Enterococcus faecium (vanA/B)
  • Staphylococcus lugdunensis
  • Candida auris
  • Cryptococcus neoformans
  • Klebsiella pneumoniae (OXA-48)
  • Escherichia coli (NDM)
  • Klebsiella pneumoniae (VIM-1)
  • Escherichia coli (mcr-1, ESBL, CTX-M)



BCID2 Positive Control 2 (six vials/pellets):

  • Candida albicans
  • Candida krusei
  • Neisseria meningitidis
  • Pseudomonas aeruginosa
  • Staphylococcus aureus (MRSA)
  • Streptococcus agalactiae (Group B)
  • Streptococcus pyogenes
  • Acinetobacter baumannii
  • Candida glabrata
  • Candida tropicalis
  • Enterobacter cloacae (CTX-M)
  • Enterococcus faecalis (vanB)
  • Escherichia coli (IMP)
  • Klebsiella oxytoca
  • Listeria monocytogenes
  • Staphylococcus epidermidis
  • Candida parapsilosis
  • Haemophilus influenzae
  • Klebisella pneumoniae (KPC)
  • Proteus vulgaris
  • Serratia marcescens
  • Streptococcus pneumoniae


BCID2 Negative Control (six vials/pellets): Blank Pellet

General Information
Documentation

General Information

Biosafety Level1
Product FormatQC Sets and Panels: Helix Elite™
Test MethodMolecular Testing
Catalog number8254
Permits and RestrictionsExport Restrictions May Apply
TaxonomyBacteria
Industry TypeClinical
DisclaimerHelix Elite QC Panels and Molecular Standards are FDA Class I exempt unassayed, in vitro diagnostic external controls, and are intended for professional laboratory use only. Results with diagnostic instruments may vary.

As 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 “8254 Blood Culture Identification Control Panel IFU"

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*The ATCC Licensed Derivative Emblem, the ATCC Licensed Derivative word mark and the ATCC catalog marks are trademarks of ATCC. Microbiologics, Inc. is licensed to use these trademarks and to sell products derived from ATCC® cultures. Look for the ATCC Licensed Derivative © Emblem for products derived from ATCC© cultures.