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  • ameridx

Ameridx Medical Equipment & Supplies In In Netherlands Antilles

4 equipment items found
Available In Netherlands AntillesNear Netherlands Antilles

AmeriDx - Model R30143011 - COVID-19 IgG/IgM Antibody Rapid Test Kit (3 lines test)

AmeriDx - Model R30143011 - COVID-19 IgG/IgM Antibody Rapid Test Kit (3 lines test)

Manufactured by:America Diagnostics, Inc.   based inSan Diego, CA 92126 USA, CALIFORNIA (USA)
This product is for in vitro diagnostic use, following guidance from the FDA for Emergency Use Authorizations of tests submitted for approval on March 16, 2020. This test has not been reviewed by the FDA and results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection ...
CONTACT SUPPLIER

AmeriDx - Model R24231213 - Calprotectin (CPTN) Rapid Test Kit, 25 Tests/pack

AmeriDx - Model R24231213 - Calprotectin (CPTN) Rapid Test Kit, 25 Tests/pack

Manufactured by:America Diagnostics, Inc.   based inSan Diego, CA 92126 USA, CALIFORNIA (USA)
The AmeriDx® Calprotectin (CPTN) Rapid Test Kit is a qualitative test that detects CPTN antigen in human fecal specimens and other body ...
CONTACT SUPPLIER

AmeriDx - Model R30142004 - H. pylori Ag Rapid Test Kit

AmeriDx - Model R30142004 - H. pylori Ag Rapid Test Kit

Manufactured by:America Diagnostics, Inc.   based inSan Diego, CA 92126 USA, CALIFORNIA (USA)
AmeriDx Fecal H. pylori Ag Rapid Test Kit is an in vitro qualitative immunochromatographic assay for the rapid detection of Helicobacter pylori (H. pylori) antigens in human stool specimen. The test results are intended to aid in the diagnosis of H. pylori infection, to monitor the effectiveness of therapeutic treatment, and to confirm the eradication of H. pylori in patients with peptic ...
CONTACT SUPPLIER

AmeriDx - Model R30143012 - COVID-19 IgG/IgM-T Antibody Rapid Test Kit

AmeriDx - Model R30143012 - COVID-19 IgG/IgM-T Antibody Rapid Test Kit

Manufactured by:America Diagnostics, Inc.   based inSan Diego, CA 92126 USA, CALIFORNIA (USA)
This product is for in vitro diagnostic use, following guidance from the FDA for Emergency Use Authorizations of tests submitted for approval on March 16, 2020. This test has not been reviewed by the FDA and results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection ...
CONTACT SUPPLIER
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