International safety notice

Aguja Bulkamid Needle, incluidas en el sistema Bulkamid® Urethral Bulking (referencia 50012).

Spain / AEMPS · ESP · Jun 16, 2021

Key facts

Title Aguja Bulkamid Needle, incluidas en el sistema Bulkamid® Urethral Bulking (referencia 50012).
Regulator Spain / AEMPS
Country ESP
Brand Aguja Bulkamid Needle, incluidas en el sistema Bulkamid® Urethral Bulking (referencia 50012).
Manufacturer Contura International A/S, Dinamarca.
Models 28022, 91.822.52.89, 05704101500128, DK-2860, 08225, 2021-349, 68956, 50012
Event type Safety Notice
Date Jun 16, 2021

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 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