8 results
·
36ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ELEVATING AND REMOVABLE LEG AND REMOVABLE ARM WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
SUTURE REMOVAL KIT
FDA 510(k)
FDA Class 2
·General Hospital
'EXMOOR' CAWOOD NASAL SPLINTS
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
BD BBL¿ MGIT¿ OADC ENRICHMENT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024
BD PROTECTOR P50
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code ONB·February 3, 2020
CAPSUREFIX
FDA Adverse Event
Injury
·MPRI·Product code NVN·February 15, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011
INTERPULSE YANKAUER TIP
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code FQH·July 29, 2014