Cardiac Care

Status™ MI

For the Rapid Qualitative Detection of Cardiac Markers to Aid in the Diagnosis of Acute Myocardiac Infarction in Human Whole Blood, Serum or Plasma.

Ordering Information

PRODUCT

# OF TESTS

ITEM #

LifeSign MI Troponin I

20

60101

LifeSign MI Myoglobin (CK-MB)/Troponin I

20

60201

LifeSign MI Cardiac Control Box

2 X 1 ml

LSC-301(a)

- OR -

• COVID-19 Anterior nasal swab – Sensitivity 93.8%, Specificity 100%
• COVID-19 Nasopharyngeal – Sensitivity 93.1%, Specificity 100%
• Flu A – Sensitivity 91.4%, Specificity 95.7%
• Flu B – Sensitivity 87.6%, Specificity 95.9%
• FDA Emergency Use Authorization (EUA)
• Visually read in 15 minutes
• Flocked nasopharyngeal swab for superior specimen collection and patient comfort

• Qualitative CK-MB, Myoglobin, Troponin
• Enables prompt Emergency Room decisions
Easy to use procedure
• Result in 15 minutes
• Reduces unnecessary testing and admissions

Our products are developed and manufactured in the USA under ISO, FDA, cGMP, and CE mark guidelines. BDSC’s team of expert sales, technical and customer service professionals are devoted to delivering the highest quality of service to our partners.

BDSC is an authorized distributor delivering high quality rapid point of care testing products to the healthcare industry. BDSC’s line of innovative products is used by clinicians to aid in the detection of medical conditions which include Infectious Disease, Women’s Health, and Cardiac Markers. The vast majority of our products are developed and manufactured in the USA under ISO, FDA, cGMP, and CE mark guidelines. BDSC’s team of sales, technical, and customer service professionals deliver the highest quality of service and support to our customers.

BDSC Company offers a range of ordering options. If you would like to speak to a BDSC expert immediately, contact us on 800-592-1041. If you prefer to enquire online, please click on ‘Get A Quote’ above.

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A Rapid Immunoassay for the Simultaneous Direct Detection and Differential Diagnosis of SAR-CoV-2, Influenza TypeA and Type B Antigen from anterior nasal and nasopharyngeal swab specimens.

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