9 results
·
28ms
·
Sources: EU EUDAMED, US FDA
FRESENIUS PURISTERIL 340 (TM)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GC Initial™
FDA UDI
Gc America Inc.·J0228745731·GC Initial™ Ti Translucent TO, 50g
CABLE CUTTER
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXZ·March 18, 2021
ABSORBABLE GAUZE PRODUCTS
FDA 510(k)
FDA Unclassified
·Unknown
AQUA TRAP
FDA 510(k)
FDA Class 1
·Anesthesiology
CARDIOPULMONARY DEVICE
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·April 22, 2014
VIRTUOSO II VR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·October 19, 2010
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code MMI·December 15, 2012
CABLE CUTTER
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HXZ·September 29, 2020