37 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTEGRIP ACETABULAR SHELL, INTEGRIP REVISION ACETABULAR SHELL
FDA 510(k)
FDA Class 2
·Orthopedic
ArgenZ HT+ 95x25 B4
FDA UDI
ARGEN CORPORATION, THE·D818122798·Dental porcelain/ceramic restoration kit
CERVIVE ANTERIOR CERVICAL PLATING SYSTEM, MODEL NUMBER 157.XXX SERIES CATALOGUE NUMBERS
FDA 510(k)
FDA Class 2
·Orthopedic
LOCKING COMPRESSION PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BD PEN NDL 32GA 4MM 14BAG 700CASE JP
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·July 10, 2019
UNKNOWN DEPUY CONSTRAINED LINER
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·June 3, 2011
MITEK BIOKNOTLESS RAPIDE (BR) W/PANACRYL
FDA Adverse Event
Malfunction
·DEPUY MITEK·Product code MAI·May 21, 2013
COAGUCHEK XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·August 14, 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
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