267 results
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30ms
·
Sources: EU EUDAMED, US FDA
MDI GLIADIN G TEST
FDA 510(k)
FDA Class 2
·Immunology
PERIARTICULAR LOCKING SCREW 3.5MM
FDA Adverse Event
Malfunction
·ZIMMER INC·Product code HWC·September 4, 2015
KINETRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·April 11, 2014
EBT ULTRAFAST CT SCANNER SYSTEM; ULTRAFAST CT SCANNER SYSTEM; C-100, C-150. C-150LXP OR C-150XP SCANNER SYSTEMS; ELECTRO
FDA 510(k)
FDA Class 2
·Radiology
DASH 3000/4000 PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
PERIARTICULAR LOCKING SCREW 3.5MM
FDA Adverse Event
Malfunction
·ZIMMER INC·Product code HWC·November 6, 2015
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·March 19, 2014
TM ANKLE TIBIAL BASE SIZE 4
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSN·November 26, 2020
TALAR COMPONENT ORANGE SIZE 4 RIGHT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSN·January 8, 2021
PROLONG TIBIAL INSERT SZ 4 +2
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HSN·January 8, 2021
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450139981·
KINETRA
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code MHY·July 30, 2012
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·January 9, 2019
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·September 26, 2018
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·December 10, 2019
ECHOTIP ULTRA HIGH DEFINITION ULTRASOUND ACCESS NEEDLE
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·July 30, 2019
NA
FDA UDI
Zimmer, Inc.·00889024057654·
NA
FDA UDI
Zimmer, Inc.·00889024058736·
MotionLoc®
FDA UDI
Zimmer, Inc.·00889024058552·
MotionLoc®
FDA UDI
Zimmer, Inc.·00889024058675·