23 results
·
21ms
·
Sources: EU EUDAMED, US FDA
EYE TRAY
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909121052·REVELATION DIAMOND 811-037SC - 5 PACK
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·34546540244339·BONE SCREWS, CROSS-FIT, SELF-TAPPING
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756021197·FINGER SPLINTS
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668110843·TIP GUARDS VENTED ASSORTED PACK OF 100
Oph. Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668122235·Gills/Welsh Cannula, 25g Angled 9mm Tip
Malibu
FDA UDI
Seaspine Orthopedics Corporation·10889981080525·Bone Probe, Extended Curved
McKesson
FDA UDI
MCKESSON MEDICAL-SURGICAL INC.·20612479275885·MASK, PROC LOOPS ASTM1 BLUE
Arthrex®
FDA UDI
ARTHREX, INC.·00888867057456·UNIVERSAL GLENOID - INLAY MEDIUM PLUS
Innonix Antiviral Child's Face Mask
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POLYVAC SURGICAL INSTRUMENT DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·July 6, 2017
GUNTHER TULIP FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·COOK INC·Product code DTK·July 6, 2017
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·May 13, 2014
REPLACEMENT HEART VALVE
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code DYE·December 1, 2010
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
LAND AMERICA HEALTH & FITNESS·Product code FSA·January 11, 2013
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017
INJECTOR N35-O
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FPA·January 7, 2021
GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET
FDA Adverse Event
Injury
·WILLIAM COOK EUROPE·Product code DTK·October 20, 2017