BioFire Diagnostics FilmArray RP2RP2 Plus Szingapúr - angol - HSA (Health Sciences Authority)

biofire diagnostics filmarray rp2rp2 plus

biomerieux singapore pte. ltd. - microbiology - the filmarray rp2/rp2 plus are multiplexed nucleic acid tests intended for use with filmarray® 2.0 or filmarray® torch systems for the simultaneous qualitative detection and identification of multiple respiratory viral and bacterial nucleic acids in nasopharyngeal swabs (nps) obtained from individuals suspected of respiratory tract infections. the following organism types and subtypes are identified using the filmarray rp2/rp2plus: adenovirus, coronavirus 229e, coronavirus hku1, coronavirus nl63, coronavirus oc43, human metapneumovirus, human rhinovirus/enterovirus, influenza a, including subtypes h1, h1-2009, and h3, influenza b, middle east respiratory syndrome coronavirus (mers-cov)- only for rp2plus, parainfluenza virus 1, parainfluenza virus 2, parainfluenza virus 3, parainfluenza virus 4, respiratory syncytial virus, bordetella parapertussis (is1001), bordetella pertussis (ptxp), chlamydia pneumoniae, mycoplasma pneumonia.

BioFire Diagnostics FilmArray Pneumonia Panel & Pneumonia Panel Plus Szingapúr - angol - HSA (Health Sciences Authority)

biofire diagnostics filmarray pneumonia panel & pneumonia panel plus

biomerieux singapore pte. ltd. - microbiology - the biofire® filmarray® pneumonia panel (biofire pneumonia panel) & pneumonia panel plus (biofire pneumonia panel plus) are multiplexed nucleic acid test intended for use with biofire® filmarray® 2.0 (biofire 2.0) or biofire® filmarray® torch (biofire torch) systems for the simultaneous detection and identification of multiple respiratory viral and bacterial nucleic acids, as well as select antimicrobial resistance genes, in sputum-like specimens (induced or expectorated sputum, or endotracheal aspirates) or bronchoalveolar lavage (bal)-like specimens (bal or mini-bal) obtained from individuals suspected of lower respiratory tract infection. the detection and identification of mers-cov is only available on the biofire® filmarray® pneumonia panel plus. the results of this test should not be used as the sole basis for diagnosis, treatment, or other patient management decisions.

Copan eSWAB Szingapúr - angol - HSA (Health Sciences Authority)

copan eswab

biomerieux singapore pte. ltd. - microbiology - copan liquid amies elution swab (eswab) collection and transport system is intended for the collection and transport of clinical specimens containing aerobes, anaerobes, fastidious bacteria, viruses and chlamydia. in the laboratory, eswab specimens can be processed, using standard clinical laboratory operating procedures, for: • bacterial culture of anaerobes, aerobes and fastidious organisms • antigens and nucleic acids detection of bacteria, viruses and chlamydia

BioFire Diagnostics FilmArray Blood Culture Identification 2 (BCID2) Panel Szingapúr - angol - HSA (Health Sciences Authority)

biofire diagnostics filmarray blood culture identification 2 (bcid2) panel

biomerieux singapore pte. ltd. - microbiology - the biofire® blood culture identification 2 (bcid2) panel is a multiplexed nucleic acid test intended for use with biofire® filmarray® 2.0 or biofire® filmarray® torch systems for the simultaneous qualitative detection and identification of multiple bacterial and yeast nucleic acids and select genetic determinants associated with antimicrobial resistance. the biofire bcid2 panel test is performed directly on blood culture samples identified as positive by a continuous monitoring blood culture system. results are intended to be interpreted in conjunction with gram stain results. the biofire bcid2 panel is indicated as an aid in the diagnosis of specific agents of bloodstream infection and results should be used in conjunction with other clinical and laboratory findings. positive results do not rule out co-infection with organisms not included in the biofire bcid2 panel. it is not intended to monitor treatment for bloodstream infection

BioFire Diagnostics Respiratory Panel 2.1 (RP2.1) Szingapúr - angol - HSA (Health Sciences Authority)

biofire diagnostics respiratory panel 2.1 (rp2.1)

biomerieux singapore pte. ltd. - microbiology - the biofire respiratory panel 2.1 (rp2.1) is a pcr- based multiplexed nucleic acid test intended for use with the biofire filmarray® 2.0 or biofire filmarray® torch systems for the simultaneous qualitative detection and identification of multiple respiratory viral and bacterial nucleic acids in nasopharyngeal swabs obtained from individuals suspected of respiratory tract infections, including covid-19. the following organism types and subtypes are identified using the biofire rp2.1:adenovirus, coronavirus 229e, coronavirus hku1,coronavirus nl63, coronavirus oc43, severe acute respiratory syndrome coronavirus 2 (sars- cov-2), human metapneumovirus, human rhinovirus/enterovirus, influenza a, including subtypes h1, h1-2009, and h3, influenza b, parainfluenza virus 1, parainfluenza virus 2, parainfluenza virus 3, parainfluenza virus 4, respiratory syncytial virus, bordetella parapertussis, bordetella pertussis, chlamydia pneumoniae, mycoplasma pneumonia.

BioFire Joint Infection (JI) Panel Szingapúr - angol - HSA (Health Sciences Authority)

biofire joint infection (ji) panel

biomerieux singapore pte. ltd. - microbiology - the biofire® joint infection (ji) panel is a multiplexed nucleic-acid-based, in vitro diagnostic test intended for use with biofire® filmarray® 2.0 and biofire® filmarray® torch systems for the simultaneous qualitative detection and identification of multiple bacterial and yeast nucleic acids and select antimicrobial resistance genes from synovial fluid obtained from individuals suspected to have a joint infection. the following organisms are identified using the biofire ji panel:gram positive bacteria, gram negative bactieria and yeast.

BioFire Diagnostics Respiratory Panel 2.1 plus (RP2.1plus) Szingapúr - angol - HSA (Health Sciences Authority)

biofire diagnostics respiratory panel 2.1 plus (rp2.1plus)

biomerieux singapore pte. ltd. - microbiology - the biofire respiratory panel 2.1 plus (rp2.1plus) is a pcr- based multiplexed nucleic acid test intended for use with the biofire filmarray® 2.0 or biofire filmarray® torch systems for the simultaneous qualitative detection and identification of multiple respiratory viral and bacterial nucleic acids in nasopharyngeal swabs obtained from individuals suspected of respiratory tract infections, including covid-19. the following organism types and subtypes are identified using the biofire rp2.1plus: adenovirus, coronavirus 229e, coronavirus hku1,coronavirus nl63, coronavirus oc43, mers-cov, sars-cov-2, human metapneumovirus, human rhinovirus/enterovirus, influenza a virus including subtypes h1, h1-2009, and h3, influenza b, parainfluenza virus 1, parainfluenza virus 2, parainfluenza virus 3, parainfluenza virus 4, respiratory syncytial virus, bordetella parapertussis, bordetella pertussis, chlamydia pneumoniae, mycoplasma pneumonia.

BioFire Diagnostics BioFire Joint Infection Panel Szingapúr - angol - HSA (Health Sciences Authority)

biofire diagnostics biofire joint infection panel

biomerieux singapore pte. ltd. - microbiology - biofire joint infection panel is a multiplexed nucleic-acid-based intended for simultaneous qualitative detection, identification of multiple bacterial, yeast nucleic acids and select antimicrobial resistance genes from synovial fluid obtained from individuals suspected to have a joint infection. the biofire ji panel is indicated as an aid in the diagnosis of specific agents of joint infection and results should be used in conjunction with other clinical and laboratory findings. the biofire ji panel is not intended to monitor treatment for joint infections.

Adaptor, blood collecting tube, single use Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

adaptor, blood collecting tube, single use

biomerieux australia pty ltd - 37566 - adaptor, blood collecting tube, single use - samplok adapter cap is intended for use to facilitate collection of blood sample into culture bottles or vacuum tubes. it is a single use device.