10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
OSTOMY BAGS URETHEROSTOMY
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209105311·KIT, TORK
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776096564·Chroma-line Suction Tube
Chameleon PTA Balloon Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TRANSPAC® IV MONITORING KIT WITH SAFESET¿ RESERVOIR AND BLOOD SAMPLING PORT, 60"
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·April 12, 2019
WAVELIGHT EX500 EXCIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·April 18, 2014
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·November 29, 2012
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code MGB·September 29, 2010
Zimmer, Cuff Tourniquet Dual Hose Single Bladder Maroon Reprocessed by Sterilmed, Sterile EO, Rx only.
FDA Enforcement
Class II
·Terminated·STERILMED, INC.·December 16, 2015