32 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Zio Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112946·CORNEAL TREPHINE BLADE8.25MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM
MDI GLIADIN G TEST
FDA 510(k)
FDA Class 2
·Immunology
PICASSO/ PICASSO LITE/ PICASSO PERIO
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·November 4, 2013
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·March 3, 2014
RESOLUTION CLIP DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MND·October 16, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC·Product code MKJ·August 28, 2013
MICRA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code PNJ·February 13, 2023
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 7, 2023
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024
GORE® VIABAHN® ENDOPROSTHESIS WITH HEPARIN BIOACTIVE SURFACE
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code NIP·May 24, 2024
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024
NI
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 20, 2024