7 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EMBOGUARD Balloon Guide Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
LIQUICHEK URINE TOXICOLOGY CONTROL (SCREEN SERIES)
FDA 510(k)
FDA Class 1
·Clinical Toxicology
ENDOLUMINAL OCCLUSION SYSTEM (EOS)
FDA 510(k)
FDA Class 2
·Cardiovascular
GREENLIGHT MOXY FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·May 30, 2014
PUMP MMT-522NAB PRDGM INS V2.2 BL EN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·November 14, 2008
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·September 6, 2011
GYNECARE PROLIFT +M ANTERIOR PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 18, 2013