7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
NON-PRESSURE AUTOCLAVE FOR STERILIZATION
FDA 510(k)
FDA Class 2
·General Hospital
Partial Pelvis Replacement
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575200832·4 hole flanges,with caudal flange
ULTRASOUND SCANNER, TYPE 1101
FDA 510(k)
FDA Class 2
·Radiology
BALANCED KNEE SYSTEM HIGH FLEX PS
FDA 510(k)
FDA Class 2
·Orthopedic
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 21, 2014
COATED VICRYL
FDA Adverse Event
Malfunction
·ETHICON, INC·Product code GAB·November 2, 2012
INTEGRIS ALLURA
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code IZI·August 27, 2010