12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Microlife Upper Arm Automatic Digital Blood Pressure Monitor
FDA 510(k)
FDA Class 2
·Cardiovascular
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00887868267239·
ORTHOPEDIC SALVAGE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304688032·
PROGLASS CEMENTS (ONE, TWO TWO LC, NINE, PLUS, SILVER)
FDA 510(k)
FDA Class 2
·Dental
NEOBLUE COZY LED PHOTOTHERAPY SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·February 20, 2020
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014
CAPSFIX PU SCR.-IN
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·June 7, 2013
RADIAL JAW¿ 4
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·July 6, 2011
BD BACTEC¿ PEDS PLUS¿/ F CULTURE VIALS (PLASTIC)
FDA Adverse Event
Malfunction
·BECTON DICKINSON CARIBE LTD.·Product code MDB·March 10, 2023
ORTHOPEDIC SALVAGE SYSTEM MAK SEGMENTAL FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·June 4, 2025
ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE TIBIAL BEARING 14MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·June 3, 2025