International safety notice

Updated Instruction for Use for Laparoscopic Manual Instruments and Accessories, Stryker Endoscopy

Germany / BfArM · DEU · Dec 16, 2014

Key facts

Title Updated Instruction for Use for Laparoscopic Manual Instruments and Accessories, Stryker Endoscopy
Regulator Germany / BfArM
Country DEU
Brand Laparoscopic Manual Instruments and Accessories, Stryker Endoscopy
Manufacturer Updated Instruction for Use for Laparoscopic Manual Instruments and Accessories, Stryker Endoscopy
Models IFU1000-401-070, 95138, 408-855-6238, 408-855-6314, 1000-401-070, IFU1000401070
Date Dec 16, 2014
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models 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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