International safety notice

Minisart Ophthalsart

Swiss / SwissMedic · CHE · Jan 19, 2021

Key facts

Title Minisart Ophthalsart
Regulator Swiss / SwissMedic
Country CHE
Brand Minisart Ophthalsart
Manufacturer Sartorius Stedim Biotech GmbH
Models 00286103, 01466103, 01321103, 00426103, 01317103, 00287103, 01189103, 00427103, 17594-GJR, 91557103, 00130103, 00588103 and 59 more
Event type Safety Notice
Date Jan 19, 2021
Regulator page fsca.swissmedic.ch

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