International safety notice

Omixon Biocomputing

United Kingdom / MHRA · GBR · Feb 10, 2020

Key facts

Title Omixon Biocomputing
Regulator United Kingdom / MHRA
Country GBR
Brand Holotype HLA 24/11 - Configuration A2 & CE v2, Holotype HLA 24/11 - Configuration A1 & CE v2, Holotype HLA 24/7 - Configuration A1 & CE v2, Holotype HLA 24/7 - Configuration A2 & CE v2
Manufacturer Omixon Biocomputing
Models 472504, 460094, FSN_QMS_446’, 447589, H52.1, 447429, 425768, 447386, QMS-446, 472509, 456287, 50-52
Event type Safety Notice
Action type Field safety notice
Date Feb 10, 2020
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices