19 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
TRI-TECH URINE SPECIMEN KIT
FDA 510(k)
FDA Class 1
·Pathology
CERAMIX PORCELAIN SYSTEM
FDA 510(k)
FDA Class 2
·Dental
APTUS 2.0/2.3 FOUR CORNER FUSION PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
GEENEN PANCREATIC STENT SET
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·January 10, 2019
UNIFY CRT-D, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·June 30, 2014
SOLOSTAR
FDA Adverse Event
Malfunction
·SANOFI-AVENTIS·Product code NSC·November 12, 2010
HEARTSTART HOME
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code NSA·December 13, 2012
GEENEN PANCREATIC STENT
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code FGE·September 14, 2018
GEENEN PANCREATIC STENT
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code FGE·September 14, 2018
GEENEN PANCREATIC STENT
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code FGE·September 14, 2018
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
ACCESS ACCUTNI+3 REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 6, 2015
UNKNOWN
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·June 9, 2021
ZIMMON PANCREATIC STENT
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·October 16, 2020