International safety notice

Gelita Medical Gelita-Spon Rapid, Gelita Ent X-Pand - tagasikutsumine, endotoksiinide kõrgem tase

Estonia / EMDDB · EST · Apr 1, 2022

Key facts

Title Gelita Medical Gelita-Spon Rapid, Gelita Ent X-Pand - tagasikutsumine, endotoksiinide kõrgem tase
Regulator Estonia / EMDDB
Country EST
Brand Gelita Medical Gelita-Spon Rapid, Gelita Ent X-Pand
Manufacturer GELITA MEDICAL GELITASPON RAPID GELITA ENT XPAND
Models 4260293130020, 90.23, 4260293130013, GE-6382, R00112, 01.10.2021, expected.2, 36.09, CR-22-002, GR-010, 180.46, RAPID3 and 3 more
Date Apr 1, 2022
Regulator page terviseamet.ee

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

Browse all International device safety notices