International safety notice

Idylla BRAF Mutation Test

Swiss / SwissMedic · CHE · Dec 20, 2022

Key facts

Title Idylla BRAF Mutation Test
Regulator Swiss / SwissMedic
Country CHE
Brand Idylla BRAF Mutation Test
Manufacturer Biocartis NV
Models „V600K, A0010, V600M”, V600E2, V600M, 15415219111324, BRAF-V600-mutierte, V600D, V600E, B1ocart1s, “V600K, V600K and 12 more
Event type Safety Notice
Date Dec 20, 2022
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice

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