7 results
·
33ms
·
Sources: EU EUDAMED, US FDA
T-TUBE WHELAN-MOSS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SALUS - Hygiene Instrument Reprocessing Container
FDA 510(k)
FDA Class 2
·General Hospital
NEGAVENT PLUS PEGASO COUGH, MODEL: DA-3 PLUS
FDA 510(k)
FDA Class 2
·Anesthesiology
VORTEK PERCUTANEOUS NEPHROSTOMY KIT WITH J CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code LJE·January 2, 2025
DTL CANN. PEDICLE+SET SCREW 6.4X50
FDA Adverse Event
Other
·ZIMMER GMBH·Product code NQP·March 23, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·October 4, 2012
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·July 22, 2010