188 results · 24ms · Sources: EU EUDAMED, US FDA

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EVERCROSS 0.035 OTW PTA DILATION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

CoRoent

FDA UDI
Nuvasive, Inc.·00887517635686·CoRoent Ant TLIF PEEK, 10x13x32mm 12°

LUCAS DENTAL CURETTE

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896052765·LUCAS DENTAL CURETTE

Portex

FDA UDI
ICU MEDICAL, INC.·15019517069884·

CODMAN BACTISEAL CATHETERS

FDA 510(k)
FDA Class 2 ·Neurology

HAC-420 HEAD ARRAY COIL

FDA 510(k)
FDA Class 2 ·Radiology

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

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE·Product code KDJ·May 9, 2013

XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·September 19, 2014