• Model / Serial
    Model Number: S-05-100-120-G3; Lot Number 01049037
  • Product Classification
  • Device Class
  • Implanted device?
  • Distribution
    Nationwide Distribution to the states of FL, NY, and PA.
  • Product Description
    IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. Indicated for palliative treatment of biliary strictures produced by malignant neoplasms
  • Manufacturer
  • 1 Event


  • Manufacturer Address
    IDEV Technologies, Inc., 253 Medical Center Blvd, Webster TX 77598-4213
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source