37 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
LYOPLANT ONLAY
FDA 510(k)
FDA Class 2
·Neurology
ArgenZ HT+ 95x25 A2
FDA UDI
ARGEN CORPORATION, THE·D818122791·Dental porcelain/ceramic restoration kit
EASYSUITE SURGICAL LIGHT CONTROL (ESLC)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNTHES ANTERIOR TENSION BAND (ATB) SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PRONOVA BLUE MONO POLY(HEXAFLUOROPROPYLENE)SUTURE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAW·May 21, 2013
ASR ACETABULAR IMPLANT 60
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 3, 2011
VITROS IMMUNODIAGNOSTIC PRODUCTS TROP I ES REAGENT PACK
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·August 13, 2008
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·May 12, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 25, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 8, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 7, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·August 27, 2020
COOK TURBO-FLO HD HEMODIALYSIS CATHETER SET
FDA Adverse Event
Injury
·COOK INC·Product code MPB·February 13, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·April 24, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·April 18, 2019
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·July 25, 2018
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·April 12, 2017
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·January 15, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Injury
·COOK INC·Product code KRA·February 17, 2020
CXI SUPPORT CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·March 18, 2021