10,000 results
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59ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LUMENX MODEL GAT-577 PHOTOCOAGU. PULSED DYE LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ALARIS® PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION·Product code FRN·May 17, 2017
ON-Q PAIN PUMP
FDA Adverse Event
Other
·I-FLOW CORP.·Product code MEB·October 15, 2010
NEXIVA 18 GA X 1-1/4 IN SINGLE PORT
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 26, 2020
HEA 1.2 BEADCHIP KIT, SLIDE
FDA Adverse Event
Malfunction
·BIOARRAY SOLUTIONS LTD.·Product code PEP·August 16, 2021
ACUVUE® OASYS® 1-DAY FOR ASTIGMATISM WITH HYDRALUXE¿ TECHNOLOGY
FDA Adverse Event
Injury
·JOHNSON & JOHNSON VISION CARE - IRELAND·Product code LPL·April 11, 2026
MASUNAGA since 1905
FDA UDI
MASUNAGA OPTICAL MFG.CO.,LTD.·04582647307675·
SYMBIQ SINGLE CHANNE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 11, 2014
SYMBIQ SINGLE CHANNEL
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·January 30, 2014
PLM APL V13.4 ABG
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·April 2, 2009
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·August 20, 2008
EXPRESSBRAID 10PK BLUE/WHITE
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HTD·May 24, 2016
PLM APL V13.4 ABG
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·April 2, 2009
ALARIS PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Injury
·CAREFUSION CORPORATION·Product code FPA·April 16, 2014
CADD MEDICATION CASSETTES
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FPA·April 28, 2022
UNICEL DXI 600 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·October 15, 2011
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·November 21, 2019
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·August 12, 2015
CADD EXTENSION SETS
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD, INC.·Product code FPA·April 28, 2022
PROTECTA XT CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012