International safety notice

Cartucho Idylla¿-BRAF Mutation Test. Referencia: A0030/6 UDI-DI:15415219111324

Spain / AEMPS · ESP · Dec 28, 2022

Key facts

Title Cartucho Idylla¿-BRAF Mutation Test. Referencia: A0030/6 UDI-DI:15415219111324
Regulator Spain / AEMPS
Country ESP
Brand Cartucho Idylla¿-BRAF Mutation Test. Referencia: A0030/6 UDI-DI:15415219111324
Manufacturer Biocartis NV, Generaal De Wittelaan 11B, 2800 Mechelen, Bélgica.
Models 58450606, V600E2, V600M, A0030, «V600K, 88170, V600R, 28022, V600M», 00005845, 91.822.52.89, V600D and 7 more
Event type Safety Notice
Date Dec 28, 2022

At a glance

  • No Recall
  • Yes Field safety notice

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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

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