QIO

Anaplasma Spp. And Ehrlichia Spp. Serological Reagents

Product code
QIO
Device name
Anaplasma Spp. And Ehrlichia Spp. Serological Reagents
Device class
Class N
Medical specialty
Unknown
Marketing pathway
Contact ODE

FDA classification definition

Tests or reagents used to detect IgG and/or IgM antibodies to Anaplasma spp. and/or Ehrlichia spp. in human serum or plasma. Used to aid in the diagnosis of either present or past infection with Anaplasma spp. and/or Ehrlichia spp. in patients suspected of exposure.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: QIO
Classification and pathway per current FDA publications. Data from openFDA (CC0).