10,000 results · 36ms · Sources: EU EUDAMED, US FDA

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VITEK® MS

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·August 11, 2017

VITEK MASS SPECTROMETER

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·October 27, 2017

VITEK MASS SPECTROMETER

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·November 27, 2017

VITEK MS INSTRUMENT

FDA Adverse Event
Malfunction ·BIOMÉRIEUX SA·Product code QBN·January 8, 2021

VITEK® MS

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·June 20, 2017

VITEK MS INSTRUMENT

FDA Adverse Event
Malfunction ·BIOMÉRIEUX SA·Product code QBN·December 11, 2020

VITEK MS

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·July 16, 2020

VITEK MASS SPECTROMETER

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·December 12, 2017

KERRISON PUNCH (GOLD TIP)

FDA Adverse Event
Injury ·AESCULAP, INC·Product code KBB·April 23, 2013

KERRISON RONGEUR, X-SMALL, SZ 0

FDA Adverse Event
Injury ·ALLEGIANCE HEALTHCARE CORP·Product code KBB·August 23, 2002

AESCULAP KERRISON RONGEUR WITH A THIN FOOTPLATE

FDA Adverse Event
Malfunction ·AESCULAP, INC.·Product code KBB·March 12, 2024

JANSON-MIDDLETON RONGEUR

FDA Adverse Event
Malfunction ·AESCULAP·Product code KBB·March 7, 1997

AESCULAP KERRISON RONGEUR WITH A THIN FOOTPLATE

FDA Adverse Event
Malfunction ·AESCULAP, INC.·Product code KBB·March 12, 2024

KERRISON RONGUER

FDA Adverse Event
Malfunction ·AESCULAP, INC·Product code KBB·September 14, 2017

VITEK® MS

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·June 17, 2020

VITEK® MS

FDA Adverse Event
Malfunction ·BIOMERIEUX, SA·Product code PEX·September 14, 2017

VITEK MS INSTRUMENT - 410895

FDA Adverse Event
Malfunction ·BIOMÉRIEUX SA·Product code QBN·November 5, 2020

C8XX2, GELPORT 120MM

FDA Adverse Event
Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·October 25, 2016

Rongeur, Nasal

FDA classification
FDA Class 1 ·Rongeur, Nasal

KBL GmbH

FDA registration
KBL GmbH·2 products·🇩🇪 Germany