307 results · 77ms · Sources: EU EUDAMED, US FDA

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MAXTER HEALTHCARE INC

FDA registration
MAXTER HEALTHCARE INC·2 products·🇺🇸 United States

Obelis s.a.

Authorized representative
🇧🇪 Belgium·546 Manufacturers·18515 Devices

SIGMA SPECTRUM

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE INC·Product code FRN·October 7, 2014

BAXTER

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE INC·Product code FPA·July 30, 2004

SPECTRUM SIGMA

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE INC·Product code FRN·August 1, 2014

SIGMA SPECTRUM

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE INC.·Product code FRN·August 19, 2014

SYRINGE PUMP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE INC·Product code FRN·April 1, 2003

BLOOD PRESSURE CUFF

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE, INC.·Product code DXQ·February 19, 1997

BAXTER COLLEAGUE IV PUMP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE, INC.·Product code FRN·November 10, 1999

DOUBLE LUMEN BREAST IMPLANT

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE. INC.·August 2, 1993

BAXTER EXTENSION SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE, INC.·Product code FPA·October 6, 2016

BAXTER COLLEAGUE IV PUMP

FDA Adverse Event
Injury ·BAXTER HEALTHCARE, INC.·Product code FRN·September 9, 1999

FOGARTY ARTERIAL EMBOLECTOMY CATHETER

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE INC.·Product code DXE·March 26, 1998

EDWARDS CRITICAL CSRE MONITOR

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE, INC·Product code MHX·May 31, 2001

Baxter Deutschland GmbH

Authorized representative
🇩🇪 Germany·6 Manufacturers

AUTOMATED PD SET

FDA Adverse Event
Malfunction ·BAXTER INTERNATIONAL INC.·Product code FKX·June 24, 2024

NXSTAGE

FDA Adverse Event
Death ·NXSTAGE MEDICAL INC., 43 SOUTH UNION ST., LAWRENCE·Product code KDI·August 12, 2023

MINICAP

FDA Adverse Event
Malfunction ·BAXTER INTERNATIONAL INC.·Product code KDJ·July 31, 2024

INTERGRATED APD SET

FDA Adverse Event
Malfunction ·BAXTER INTERNATIONAL INC.·Product code FKX·July 15, 2024

AMIA AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Malfunction ·BAXTER INTERNATIONAL INC·Product code FKX·July 18, 2024