12 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
DUAL LUMEN 5 FR PERIP CENT VEN CATH W/GROSHONG VAL
FDA 510(k)
FDA Class 2
·General Hospital
ORTHOTM Sera Anti-Leb Blood Grouping Reagent
FDA UDI
ALBA BIOSCIENCE LIMITED·10758750013111·The Anti-Leb reagent (Anti-LE2) is for the qual...
ORA Implant Abutment 4.0mm Cuff (AE)
FDA UDI
STERNGOLD DENTAL LLC·00841549111907·The ORA System is indicated for use with dental...
GIOTTO MAMMOGRAPHY HF
FDA 510(k)
FDA Class 2
·Radiology
PERTAC BOND
FDA 510(k)
FDA Class 2
·Dental
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/10 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·February 24, 2021
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019
GREEN RELOAD
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 22, 2010
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 1, 2014
LIFEVEST WCD 3000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·November 30, 2012
UNKNOWN HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018