106 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MYOCARDIAL PROTECTION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Convaid
FDA UDI
CONVAID PRODUCTS, INC.·00840117408685·
Sklar®
FDA UDI
SKLAR CORPORATION·10649111102981·SIMS CURETTE MALL SHARP #0
Arrow Epidural Needle KZ-05500-007(Luer); KZ-05500-009 (NRFit)
FDA 510(k)
FDA Class 2
·Anesthesiology
CHLORIDE REAGENT FOR THE AU5000 CLINICAL LAB. ANA.
FDA 510(k)
FDA Class 2
·Clinical Chemistry
AR-1600G AUTO-REFRACTOMETER
FDA 510(k)
FDA Class 1
·Ophthalmic
EPIDURAL CATHETERIZATION SET
FDA Adverse Event
Malfunction
·Product code CAZ·July 17, 2020
EPIDURAL CATHETERIZATION SETS
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code BSO·January 22, 2020
EPIDURAL CATHETERIZATION KIT
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code BSO·March 17, 2020
EPIDURAL CATHETERIZATION KIT: 19 GA
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code CAZ·April 17, 2017
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020
INTERMITTENT
FDA Adverse Event
Injury
·UNOMEDICAL S.R.O.·Product code KOD·September 21, 2020