BIOFIRE® Respiratory Panel 2.1 plus with SARS-CoV-2 is CE marked
15 Julho 2020 - 2:00AM
Business Wire
Regulatory News:
bioMérieux (Paris:BIM), a world leader in the field of in vitro
diagnostics, today announced that the BIOFIRE® Respiratory Panel
2.1 plus (RP2.1plus) is CE marked. The BIOFIRE® Respiratory Panel
2.1 plus (RP2.1plus) tests for 23 pathogens (19 viruses, including
SARS-CoV-2, and 4 bacteria) responsible for the most frequent
respiratory tract infections. It will be commercially available in
all countries that recognize CE marking from now on or shortly
thereafter .
The BIOFIRE® RP2.1plus advances the existing BIOFIRE®
Respiratory Panel 2 plus (RP2plus) by adding SARS-CoV-2 to the
panel menu while maintaining an assay runtime of about 45 minutes.
The BIOFIRE® RP2.1plus panel also includes an assay for the Middle
East Respiratory Syndrome Coronavirus (MERS-CoV). This new panel
allows healthcare providers to quickly identify patients with
common respiratory pathogens and differentiate those with COVID-19,
using one single test. The BIOFIRE® RP2.1plus runs on the fully
automated BIOFIRE® FILMARRAY® 2.0 and BIOFIRE® FILMARRAY® TORCH
systems and is extremely easy to use.
“The availability of BIOFIRE® RP2.1plus in all countries
recognizing CE marking represents a global syndromic response to
this unprecedented COVID-19 pandemic,” said Pierre Boulud, Chief
Operating Officer, Executive Vice President, Clinical Operations at
bioMérieux. “With increasing reagent production capacity and an
installed base of more than 14 000 BIOFIRE® units throughout the
world, BIOFIRE® RP2.1plus will play a key role now and in the
upcoming respiratory season as healthcare providers face the
regular group of respiratory pathogens as well as SARS-CoV-2”, he
added.
The BIOFIRE® RP2.1plus Panel is part of a suite of products in
response to the COVID - 19 pandemic. The ARGENE® SARS-CoV-2 R-GENE®
was launched in March 2020, followed by the U.S. FDA EUA cleared
BIOFIRE® RP2.1 panel and the VIDAS® anti-SARS- CoV-2 IgM and
anti-SARS-CoV-2 IgG tests. These complementary tests help meet the
varying needs of bioMérieux’s diverse customers and patients
throughout the world.
About the BIOFIRE® solution
The BIOFIRE® solution is a U.S. FDA-cleared and CE-marked
multiplex PCR closed and fully-automated system that integrates
sample preparation, amplification, and detection. A BIOFIRE® test
requires only two minutes of hands-on time and has a total run time
of about 45 to 75 minutes, depending on the panel.
The BIOFIRE® range has the largest infectious disease pathogen
menu commercially available composed of:
- BIOFIRE® Respiratory Panels (RP, RP2, RP2plus, RP2.1 and
RP2.1plus), identifying between 20 and 23 respiratory viruses and
bacteria performed directly on nasopharyngeal swabs in transport
media.
- BIOFIRE® COVID-19 test detects SARS-CoV-2 in approximately 45
minutes from a nasopharyngeal swab in transport media.
- BIOFIRE® RP EZ, identifying 11 viral and 3 bacterial pathogens
associated with respiratory infections. FDA-cleared and CLIA-waived
for use in the US only.
- BIOFIRE® Pneumonia (PN) and Pneumonia plus (PNplus) Panels,
identifying 33 to 34 targets (18 bacteria, 8 to 9 viruses, 7
resistance genes to antibiotics) in sputum (including endotracheal
aspirate) and bronchoalveolar lavage (including mini-BAL). 15 of
the bacterial targets are reported with semi-quantitative
information about the abundance of organisms in a given
sample.
- BIOFIRE® Blood Culture Identification 2 (BCID2), identifying 43
of the most common causes of bloodstream infections and associated
antimicrobial resistances directly from positive blood
culture.
- BIOFIRE® Gastrointestinal (GI) Panel, identifying 22 of the
most common viral, bacterial, and parasitic causes of infectious
diarrhea directly from stool in Cary Blair transport media.
- BIOFIRE® Meningitis/Encephalitis (ME) Panel, identifying 14
bacterial, viral, and fungal causes of meningitis and encephalitis
directly from cerebrospinal fluid.
ABOUT BIOMÉRIEUX
Pioneering Diagnostics
A world leader in the field of in vitro diagnostics for over 55
years, bioMérieux is present in 44 countries and serves more than
160 countries with the support of a large network of distributors.
In 2019, revenues reached €2.7 billion, with over 90% of
international sales.
bioMérieux provides diagnostic solutions (systems, reagents,
software and services) which determine the source of disease and
contamination to improve patient health and ensure consumer safety.
Its products are mainly used for diagnosing infectious diseases.
They are also used for detecting microorganisms in agri-food,
pharmaceutical and cosmetic products.
bioMérieux is listed on the Euronext Paris
stock market.
Symbol: BIM – ISIN Code: FR0013280286
Reuters: BIOX.PA/Bloomberg: BIM.FP
Corporate website: www.biomerieux.com.
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version on businesswire.com: https://www.businesswire.com/news/home/20200714005985/en/
Investor Relations bioMérieux Sylvain Morgeau
Tel.: + 33 4 78 87 51 36 investor.relations@biomerieux.com
Media Relations bioMérieux Aurore Sergeant Tel.: +
33 4 78 87 21 99 media@biomerieux.com
Image Sept Laurence Heilbronn Tel.: + 33 1 53 70 74 64
lheilbronn@image7.fr
Claire Doligez Tel.: + 33 1 53 70 74 48 cdoligez@image7.fr
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