13 results
·
31ms
·
Sources: EU EUDAMED, US FDA
ACTEGY LTD.
FDA registration
ACTEGY LTD.·6 products·🇬🇧 United Kingdom
REVITIVE IX
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 30, 2018
REVITIVE ARTHRITIS KNEE
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NGX·October 5, 2018
REVITIVE
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NGX·November 6, 2018
CBV3
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 30, 2018
REVITIVE IX
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 29, 2018
REVITIVE MEDIC
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NGX·November 8, 2018
CBV3
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 30, 2018
REVITIVE MEDIC
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 31, 2018
AEROSURE MEDIC
FDA Adverse Event
Death
·ACTEGY LTD·Product code BWF·May 31, 2018
REVITIVE MEDIC 2469MD
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 30, 2018
REVITIVE DX
FDA Adverse Event
Injury
·ACTEGY LTD·Product code NUH·May 31, 2018
MDSS GmbH
Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices