122 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SIMPLEXA FLU A/B & RSV
FDA 510(k)
FDA Class 2
·Microbiology
REPICCI II RESURFACING KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304449909·
Orthopaedic Surgical Instruments
FDA UDI
CITIEFFE SRL·08056711921259·
Tibial Tower
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215056612·
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800113904729·VICEROY Rod - 5.5 (D)5.5x(L)170mm
MODEL 9000 PEDIATRIC WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
DIGORA PCT
FDA 510(k)
FDA Class 2
·Dental
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 17, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·October 7, 2020
LIGASURE
FDA Adverse Event
Injury
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·July 21, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 20, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 26, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·June 9, 2021
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·February 2, 2018
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·November 13, 2018
GMK REVISION TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·January 15, 2026
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MEDICAL PRODUCTS·Product code GEI·April 16, 2019
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·April 24, 2020
LIGASURE
FDA Adverse Event
Malfunction
·COVIDIEN MFG DC BOULDER·Product code GEI·March 14, 2019
GMK PRIMARY TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 30, 2025