Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA).
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity.
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Manufacturer's By Device Histoplasma capsulatum antigen IVD kit enzyme immunoassay (EIA)-Histoplasma capsulatum antigen IVD kit enzyme immunoassay (EIA)
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
MiraVista Diagnostics LLC
4705 Decatur Blvd.
Indianapolis
Indiana 46241
United States
UKCApartner4U Limited
7 CAMPION WAY
BINGHAM NOTTINGHAM
NG13 8 TR
England United Kingdom
12/29/2021
21554