International safety notice

Kit de tipificación de HLA Olerup QTYPE 11, Nº de catálogo 201.701-03/10.

Spain / AEMPS · ESP · Sep 12, 2022

Key facts

Title Kit de tipificación de HLA Olerup QTYPE 11, Nº de catálogo 201.701-03/10.
Regulator Spain / AEMPS
Country ESP
Brand Kit de tipificación de HLA Olerup QTYPE 11, Nº de catálogo 201.701-03/10.
Manufacturer CareDx AB, Suecia
Models ATENCI6N, RESOLUCI6N, 91.822.52.89, SEROL6GICA, SEROL6AICO, 201.701-03, ACCI6N?, ACCI6N, DETERMINACI6N, TIPIFIC6, GESTI6N, 2022-04 and 39 more
Event type Safety Notice
Date Sep 12, 2022

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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