7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EXTENSION SET WITH ANTI-SIPHON VALVE
FDA 510(k)
FDA Class 2
·General Hospital
MyoSEPCT ES to MyoSPECT Upgrade
FDA UDI
G E MEDICAL SYSTEMS ISRAEL LTD.·00195278722546·MyoSPECT ES to MyoSPECT Upgrade kit
K-Bond Universal
FDA 510(k)
FDA Class 2
·Dental
IMMUNOCARD STAT! RSV MODEL #750630
FDA 510(k)
FDA Class 1
·Microbiology
LIGASURE ATLAS HANDSWITCHING 37CM
FDA Adverse Event
Malfunction
·COVIDIEN LLC (SHANGHAI)·Product code GEI·April 16, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·February 4, 2013
FOOTPRINT PEEK 4.5 M
FDA Adverse Event
Malfunction
·SMITH & NEPHEW ENDOSCOPY·Product code MBI·December 29, 2010