Szybki test diagnostyczny COMBO 10w1 BISAF w opakowaniu jednostkowym, profesjonalny test kasetkowy do wykrywania wielu patogenów, obok widoczna kasetka testowa

Szybki test diagnostyczny COMBO 10w1 BISAF w opakowaniu jednostkowym, profesjonalny test antygenowy do wykrywania wielu patogenów

Kasetka testowa BISAF COMBO 10w1 zapakowana w szczelne, foliowe opakowanie ochronne.

Opakowanie szybkiego testu antygenowego BISAF COMBO 10w1 przedstawione pod kątem.

Opakowanie szybkiego testu antygenowego BISAF COMBO 10w1 – widok poziomy.

Tylna strona opakowania szybkiego testu antygenowego BISAF COMBO 10w1 z informacjami o zawartości zestawu i producencie.

Probówka z buforem ekstrakcyjnym oraz końcówką kroplomierza – element zestawu testowego BISAF COMBO 10w1.

Sterylna wymazówka nosogardzielowa w indywidualnym, foliowym opakowaniu – element zestawu testowego BISAF COMBO 10w1.

BISAF COMBO 10in1 test | SARS-CoV-2 | Influenza A+B | RSV | ADV | hMPV | RhV | hPIV | Mycoplasma pneumoniae | Streptococcus pneumoniae | 1 piece

32,19 PLN

34,99 PLN (incl. 8% VAT)

Product intended for professional use.

Availability: In stock

Product description

BISAF COMBO 10in1 test (nasopharyngeal swab)

This is a rapid test intended for the qualitative and differential detection of antigens of SARS-CoV-2, influenza virus types A and B, respiratory syncytial virus (RSV), adenovirus (ADV), human metapneumovirus (hMPV), human rhinovirus (RhV), humen parainfluenza virus (hPIV), as well as the bacteria Mycoplasma pneumoniae and Streptococcus pneumoniae. The tested sample is collected from the patient’s nasopharynx. The test is available as a single-unit package.

1 swab = 10 results

The high sensitivity and specificity of this test ensure reliable and accurate results, available in just 15 minutes!

For professional use only.

This is a medical device. Use it in accordance with the instructions for use or the label.

Properties

sample material: nasopharyngeal swab
painless sample collection
high-quality product
rapid results in just 15 minutes
single packaging
intended for professional use

Test specification

SARS-CoV-2: sensitivity: 97,17%, specificity: 99,56%, accuracy: 99,24%
Influenza A: sensitivity: 94,83%, specificity: 99,31%, accuracy: 98,98%
Influenza B: sensitivity: 93,94%, specificity: 99,47%, accuracy: 99,24%
RSV: sensitivity: 97,35%, specificity: 99,41%, accuracy: 99,11%
ADV: sensitivity: 98,53%, specificity: 99,17%, accuracy: 99,11%
hMPV: sensitivity: 95,24%, specificity: 99,42%, accuracy:98,86%
RhV: sensitivity: 95,65%, specificity: 99,7%, accuracy: 99,11%
hPIV: sensitivity: 96,47%, specificity: 99,43%, accuracy: 99,11%
Mycoplasma pneumoniae: sensitivity: 97,39%, specificity: 99,70%, accuracy: 99,36%
Streptococcus pneumoniae: sensitivity: 95,65%, specificity: 99,81%, accuracy: 99,41%

The package contains

test cassette
single-use sterile swab
extraction buffer
user manual

Application

general practitioners (family medicine) – the test enables rapid assessment of the severity of inflammation in patients presenting with symptoms of infection, supporting decisions on further diagnostics, observation, or initiation of treatment, including the appropriateness of antibiotic therapy.
pediatricians – semi-quantitative CRP determination allows differentiation between viral and bacterial infections in children and enables monitoring of inflammatory dynamics without the immediate need for laboratory referral.
infectious disease specialists – the test serves as a rapid tool supporting the assessment of inflammatory activity during acute infections and the evaluation of the body’s response to the applied treatment.
hospital wards and emergency departments (ED) – the short time to result allows for efficient initial patient assessment, supporting decisions regarding hospitalization, further laboratory testing, or outpatient treatment.
long-term care facilities and nursing homes – regular monitoring of CRP levels enables early detection of inflammatory conditions in chronically ill patients and assessment of treatment effectiveness.
procedure rooms and diagnostic points – the simplicity of the test and the ability to use whole blood, serum, or plasma make it well suited for outpatient settings, providing fast and reliable diagnostic support.

Product identification data and responsible entities

EAN code: 6937339203700

Manufacturer	Authorized representative	Importer / Distributor
VivaChek Biotech (Hangzhou) Co., Ltd. Level 2, Block 2, 146 East Chaofeng Rd., Yuhang Economy Development Zone, Hangzhou, Zhejiang, 311100, China info@vivachek.com www.vivachek.com	CMC Medical Devices Drugs, S.L. Calle Horacio Lengo 18 29006 Málaga Spain info@cmcmedicaldevices.com	Bisaf Sp. z o.o. Rdestowa 5 54-530 Wrocław Polska 24h@bisaf.pl +48 503411527 www.bisaf.pl