International safety notice

Safety Notice concerning user instructions for laser device Dornier Medilas D UroBeam, Dornier MedTech Laser GmbH

Germany / BfArM · DEU · Feb 22, 2011

Key facts

Title Safety Notice concerning user instructions for laser device Dornier Medilas D UroBeam, Dornier MedTech Laser GmbH
Regulator Germany / BfArM
Country DEU
Brand laser device Dornier Medilas D UroBeam, Dornier MedTech Laser GmbH
Manufacturer Safety Notice concerning user instructions for laser device Dornier Medilas D UroBeam, Dornier MedTech Laser GmbH
Models 75-7212088, 8153-888-179, 17.JANUAR, 20580, 888-151, 812149854, 14520, D-82234, 55780751, 888-212, JAN.2010
Date Feb 22, 2011
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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

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