7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EMIT-AND METHOTREXATE ASSAY
FDA 510(k)
FDA Unclassified
·Unknown
WUJIN #3 FEMORAL BONE PLATE
FDA 510(k)
FDA Class 2
·Orthopedic
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, LIGHT YELLOW COLOR
FDA 510(k)
FDA Class 1
·General Hospital
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/14 MM L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·February 10, 2022
LIGACLIP CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDO·May 15, 2014
CAPSUREFIX NOVUS MRI
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code NVN·October 31, 2012
STRETCHER
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV·Product code FPO·August 17, 2010