30 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VIRTUOSO SYSTEM FOR IHC PR (IE2)
FDA 510(k)
FDA Class 2
·Hematology
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-PIPERACILLIN-TAZOBACTAM (GP) 1/4-128/4 UG/ML
FDA 510(k)
FDA Class 2
·Microbiology
PROGLASS CEMENTS (ONE, TWO TWO LC, NINE, PLUS, SILVER)
FDA 510(k)
FDA Class 2
·Dental
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929066300·Corpectomy, 16Dx18Wx69H 0°
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929066614·Corpectomy, 16Dx18Wx69H 6°
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 8, 2024
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code MTA·July 8, 2011
ALTRX NEUT 28IDX50OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 10, 2014
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
UNKNOWN PLATE
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 21, 2026
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·May 7, 2018
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017