187 results · 21ms · Sources: EU EUDAMED, US FDA

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LIFEBRIDGE

FDA 510(k)
FDA Class 2 ·Cardiovascular

TARTAR REMOVER FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896052888·TARTAR REMOVER FORCEPS SMALL SIZE TUNGSTEN CARB...

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973530·

DISPOSABLE PROPHY ANGLE; DISPOSABLE PROPHY ANGLE

FDA 510(k)
FDA Class 1 ·Dental

ASAHI ASTATO XS 20 PERIPHERAL GUIDE WIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

AMISTEM H CEMENTLESS STEM SIZE 2 STD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·December 11, 2014

STEM: AMISTEM H HA COATED STD STEM SIZE 2

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 31, 2020

VERSAFITCUP CC TRIO ACETABULAR SHELL CC TRIO Ø 54

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 4, 2019

VERSAFITCUP CC TRIO ACETABULAR SHELL

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 3, 2017

AMISTEM H, HA COATED STEM SIZE 5 STD

FDA Adverse Event
Death ·MEDACTA INTERNATIONAL SA·Product code LZO·September 20, 2017

AMISTEM H FEMORAL CEMENTLESS STEM SIZE 3 STD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·December 12, 2013

QUADRA-S CEMENTLESS, SAND BLASTED LAT STEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL, SA·Product code JDI·July 29, 2015

STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 4

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·July 11, 2019

VERSAFITCUP CC CUP IMPACTOR

FDA Adverse Event
Malfunction ·MEDACTA INTERNATIONAL, SA·Product code LXH·November 21, 2014

STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 4

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·December 2, 2019

STEM: QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 5

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·March 18, 2020

VERSAFITCUP ACETABULAR SHELL CC TRIO Ø 56

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 9, 2018

DEPUY ASR XL FEM IMP SIZE 39

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·May 9, 2013

530G INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 19, 2014

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 17, 2011