International safety notice

FH Ortho BePod percutaneous screw - ebakorrektne kasutusjuhendi tõlge

Estonia / EMDDB · EST · Dec 1, 2020

Key facts

Title FH Ortho BePod percutaneous screw - ebakorrektne kasutusjuhendi tõlge
Regulator Estonia / EMDDB
Country EST
Brand FH Ortho BePod percutaneous screw
Manufacturer FH ORTHO BEPOD PERCUTANEOUS SCREW
Models 270689, 270688, 270686, 264247, 264249, 268415, 264241, 270687, 267829, 256454, 268413, GLB100563 and 46 more
Date Dec 1, 2020
Regulator page terviseamet.ee

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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