3,257 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EO IMPL., Ø 3.3 / 3.5MM, SLA 5.0MM
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code KCZ·November 8, 2021
BRAVA BRA
FDA Adverse Event
Other
·BRAVA, LLC·Product code KCZ·March 1, 2002
AMOENA
FDA Adverse Event
Injury
·COLOPLAST CORP.·Product code KCZ·November 3, 2000
AMOENA
FDA Adverse Event
Injury
·COLOPLAST·Product code KCZ·October 24, 2000
BREAST PROSTHESIS
FDA Adverse Event
Malfunction
·MCGHAN TEXTURE BREAST PROSTH.·Product code KCZ·April 27, 1993
BREAST PROSTHESIS
FDA Adverse Event
Malfunction
·DOW CORNING·Product code KCZ·April 27, 1993
JODEE BRA
FDA Adverse Event
Malfunction
·JODEE BRA, INC.·Product code KCZ·July 30, 1998
AMOENA
FDA Adverse Event
Injury
·COLOPLAST CORP·Product code KCZ·June 13, 1998
EO IMPL., Ø 3.3 / 3.5MM, SLA 5.0MM
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code KCZ·January 4, 2024
MAMMARY PROSTHESIS
FDA Adverse Event
Injury
·MENTOR·Product code KCZ·July 23, 1993
NATURAL WEAR BREAST FORMS
FDA Adverse Event
Malfunction
·CAMP INTERNATIONAL INC.·Product code KCZ·January 24, 1997
EO IMPL., 3.3 / 5.5MM, SLA 2.5MM
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code KCZ·March 8, 2021
EO IMPL., Ø 3.3 / 3.5MM, SLA 5.0MM
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code KCZ·January 20, 2022
BREAST IMPLANTS
FDA Adverse Event
Injury
·DOW CORNING MAMMARY IMPLANTS·Product code KCZ·January 26, 1993
Centurion-Trays EBSI1021 VALVE CHANGE KIT- DOUBLE
FDA Recall
Terminated
·Centurion Medical Products Corporation·Product code KCZ·December 11, 2019
Prosthesis, Breast, External, Used With Adhesive
FDA classification
FDA Class 1
·Prosthesis, Breast, External, Used With Adhesive
Kaz
FDA UDI
KAZ USA, INC.·00328785201062·HUMIDIFIER, HOSPITAL, 4100
Kaz
FDA UDI
KAZ USA, INC.·00328785001471·HUMIDIFIER, IMPELLER,1 GL.
Kaz
FDA UDI
KAZ USA, INC.·00328785000450·Thermometer, Clear, Digital
Kaz
FDA UDI
KAZ USA, INC.·00328785221008·VAPORIZER,1GL,N/L,6-PACK