37 results · 23ms · Sources: EU EUDAMED, 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