Diamedix Corporation

3 devices in the database

  • Model / Serial
    The kit lot number is 42003. The conjugate lot number is 42023.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distributed to 54 laboratory accounts throughout the US.
  • Product Description
    The Is-Syphilis TREP-CHEK (TM) Test Kit is a confirmatory in vitro enzyme immunoassay for the qualitative detection of Treponema pallidum IgG antibodies in human serum or plasma. The reagents can be used either manually or in conjunction with the MAGO Plus or APTUS Automated EIA Processors. The FDA has not cleared this product for use in screening blood or plasma donors. || The kit is labeled with an expiration date of Mar 04 and requires storage at 2-8 degree Centigrade.The non conforming kit component is the Conjugate that consists of a glass bottle with red cap containing 30 ml goat anti-human IgG labeled with horseradish peroxidase.
  • Model / Serial
    Lot # 91803Z and 30804/30804Z
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Distributed to Domestic customers only.
  • Product Description
    The Is-Legionella IgG/IgM/IgA test kits are packaged in cardboard boxes with individual components secured within a foam insert.
  • Model / Serial
    Lot Number 71303, expiration date June 2004
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Product was distributed to three hospitals/clinics in AZ, CA and TX.
  • Product Description
    Product is packaged in a box and is labeled: Syphilis TREP-CHEK No. 720-100-10, 960 test, For in Vitro Diagnostic Use Lot 71303 Exp. Jun 04 Diamedix, A subsidiary of IVAX Diagnostics, Inc. MIAMI, FL 33127

2 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    Diamedix Corporation, 14100 Nw 57th Ct, Miami Lakes FL 33014-3107
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • Manufacturer Address
    Diamedix Corporation, 2140 N. Miami Avenue, Miami FL 33127
  • Source
    USFDA