International safety notice

Diagnostické zdravotnické prostředky in vitro

Czech / Ksrzis · CZE · Feb 25, 2019

Key facts

Title Diagnostické zdravotnické prostředky in vitro
Regulator Czech / Ksrzis
Country CZE
Brand ORG 248 Alegria® anti-MCV
Manufacturer ORGENTEC Diagnostika GmbH, Německo
Models 1705292, 55129, 31192, 550400220200, 1706145, 49-51, 6131-92, 248LOT, 706561, 2018-07-31, 100352, 55134 and 15 more
Event type Safety Notice
Date Feb 25, 2019
Regulator page eregpublicsecure.ksrzis.cz

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