29 results · 53ms · Sources: EU EUDAMED, US FDA

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DYNATORQUE ATTACHMENT

FDA Adverse Event
Other ·PRO-DEX MICRO MOTORS INC.·Product code EFB·October 15, 2013

MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HBC·January 20, 2017

MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HBC·January 20, 2017

SANAO

FDA Adverse Event
Injury ·SCICAN GMBH·Product code EGS·March 20, 2015

1/2 SIZE PERF BASKET LID 247X257MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code FSM·June 8, 2017

1/2 SIZE PERF BASKET LID 247X257MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code FSM·June 8, 2017

1/2 SIZE PERF BASKET LID 247X257MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code FSM·June 8, 2017

MICROSPEED UNI MICRO 150 MOTOR

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HBC·April 7, 2016

MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 10, 2022

MICROSPEED UNI CONTROL UNIT W/COOL.UNIT

FDA Adverse Event
Malfunction ·AESCULAP AG & CO. KG·Product code HBC·July 3, 2008

MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HWE·June 8, 2017

MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HWE·June 8, 2017

MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HWE·June 8, 2017

MICRO-LINE STRAIGHT HDPC 1:1 ROUND SHAFT

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HWE·June 21, 2017

Medtronic microTargeting Drive Motor Option used with the micro Targeting Drive System with models: 9033G0711; 9033G0712; 9033G0713; 9033G0811 and FHC 1008-66

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·October 31, 2005

MICRO-LINE STRAIGHT HDPC 1:1 F/2.35X70MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HWE·March 2, 2016

FHC microTargeting Power Assist System used with the micro Targeting Drive System, models: 66-DA-ME; 66EL-MC; 66EL-MS;66EL-MS-02; 66-EL-MS-03; 66-EL-RM; MT-DS-AM; MT-DS-MD.

FDA Recall
Terminated ·FHC, Inc.·Product code HAW·October 31, 2005

A1A-2000

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·March 29, 2018

PUMP MMT-1781K 670G V4.11 MG

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·September 3, 2021

DAVINCI X

FDA Adverse Event
Injury ·INTUITIVE SURGICAL, INC·Product code NAY·October 18, 2023