BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot Recall for Nimbus Pico µ, ClearStream Technologies Ltd.

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01916/10

The manufacturer ClearStream Technologies Ltd. recalls one lot each of two percutaneous transluminal coronary angioplasty catheter designated Nimbus Pico µ. The balloon size of the catheters are different to the balloon size indicated on the device labels.

Advisory Notice only available in German language.

Lot Recall for Nimbus Pico µ, ClearStream Technologies Ltd. , Download_VeroeffentlichtAm_EN PDF, 65KB, File is accessible

Use of cookies

Cookies help us to provide our services. By using our website you agree that we can use cookies. Read more about our Privacy Policy and visit the following link: Privacy Policy (only in German)

OK