3,257 results · 34ms · Sources: EU EUDAMED, US FDA

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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