9 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MRXperion MR Injection System, MRXperion MR Injection System Syringe Kit
FDA 510(k)
FDA Class 2
·Cardiovascular
HARDYDISK AST CEFTAROLINE, 30 UG MODEL Z939
FDA 510(k)
FDA Class 2
·Microbiology
HYPERTRANSIT INFUSION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
TECNIS
FDA Adverse Event
Injury
·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQL·September 6, 2018
VALEO / VALEO II
FDA Adverse Event
Malfunction
·SINTX TECHNOLOGIES (FORMERLY AMEDICA CORP)·Product code MAX·March 25, 2020
S-ROM M HEAD 36MM +3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 6, 2014
TALENT TAA
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·June 3, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 2, 2011
2.8MM Q-FIX ALL SUTURE ANCHOR
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code MBI·October 9, 2024