10 results
·
30ms
·
Sources: EU EUDAMED, US FDA
ENGSTROM ELIZA DUO CO2 & O2 ANALYZ
FDA 510(k)
FDA Class 2
·Anesthesiology
GIBRALT ROD-TO-ROD CROSS CONNECTORS
FDA 510(k)
FDA Class 2
·Orthopedic
DERMAGRIP-G, AND MULTIPLE CUSTOMERS TRADE NAME GREEN, ALOE VERA COATED, POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEI
FDA 510(k)
FDA Class 1
·General Hospital
OXFORD PH3 CEMENTLESS FEM SZ L
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·December 15, 2017
OXF UNI CMNTLS TIB SZ F RM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·December 15, 2017
OXF ANAT BRG RT LG SIZE 5 PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·December 15, 2017
DXTEND SCREW LOCK D4.5X30MM
FDA Adverse Event
Injury
·DEPUY FRANCE S.A.S.-SAINT PRIEST 3003895575·Product code KWS·May 30, 2014
PROSTAR XL SUTURE-MEDIATED CLOSURE
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·November 20, 2012
TERUMO CDI 540 CALIBRATOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 17, 2010
VERSYS FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER, TURPEAUX INDUSTRIAL PARK·Product code JDI·March 31, 2016