8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Restoration Anatomic Shell
FDA 510(k)
FDA Class 2
·Orthopedic
Oticon
FDA UDI
Oticon A/S·05707131288660·RIA2 PRO, DESIGNRITE 10 WL CRED
Prolift Post-Pack Instruments
FDA UDI
Life Spine, Inc.·00190837031909·
TEMPUS IC PROFESSIONAL PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
COMFORT AND INSET SUBCUTANEOUS INFUSION SETS FOR USE WITH ABBOTT INFUSION PUMPS
FDA 510(k)
FDA Class 2
·General Hospital
BIOMET CC CRUCIATE TRAY 79MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·October 8, 2014
UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·June 7, 2013
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 30, 2011