179 results
·
26ms
·
Sources: EU EUDAMED, US FDA
ESCREEN SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Toxicology
TruForm
FDA UDI
Rmo, Inc.·00885797099846·MN 1ST BI BD KT N/L R/L 134
RMO
FDA UDI
Rmo, Inc.·00885797100290·DUAL-TOP TAD SYSTEM KIT
SCANLAN® Needle Holders
FDA UDI
SCANLAN INTERNATIONAL INC·00846159031591·LEGACY Jacobson Titanium Micro Needle Holder
JMS A.V. FISTULA NEEDLE SET ACCORDION TYPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
REAADS IGG ANTI-PROTHROMBIN SEMI-QUANTITATIVE TEST KIT
FDA 510(k)
FDA Class 2
·Immunology
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
RETRACTOR
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code GAD·February 28, 2013
ENDOPLEGE CORONARY SINUS CATHETER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DWF·March 1, 2011