BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis

2006.12.20

Product group Optics / Precision engineering
Reference 03102/06

The company Lumenis issued an information concerning the recall of Lumenis DuoTome SideLite™ 550 Micron Delivery System. The recall was initiated due to the absence of the black indicator markings on the metal tip and fiber degradation during use.

Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis , Download_VeroeffentlichtAm_EN PDF, 107KB, File does not meet accessibility standards

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