International safety notice

Zdravotnické prostředky pro jednorázové použití

Czech / Ksrzis · CZE · Jul 28, 2017

Key facts

Title Zdravotnické prostředky pro jednorázové použití
Regulator Czech / Ksrzis
Country CZE
Brand Percuvance® Percutaneous Surgical System
Manufacturer Teleflex Medical
Models 73L1600025, 73E1600341, 73G1600726, 73F1600206, 73G1600015, 73L1600559, 73B1700525, 73D1600483, 73G1600016, 73H1600147, 73C1600454, 73K1600501 and 97 more
Event type Safety Notice
Date Jul 28, 2017
Regulator page eregpublicsecure.ksrzis.cz

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

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