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