32 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EBW NM 2.0
FDA 510(k)
FDA Class 2
·Radiology
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964096877·Endo Carry-On Procedure Kit
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964099274·The ENDO CARRY-ON Procedure Kit contains all of...
E1 AVANTAGE HEAD
FDA 510(k)
FDA Class 2
·Orthopedic
PRIMARY SOLUTION SET WITH UNIVERSAL SPIKE, INJECTION SITE AND MALE LUER LOCK
FDA 510(k)
FDA Class 2
·General Hospital
BD PLASTIPAK 3ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code FMF·August 7, 2023
BD PLASTIPAK 3ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code FMF·August 7, 2023
BD PLASTIPAK 3ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code FMF·August 7, 2023
BD PLASTIPAK 3ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY·Product code FMF·August 7, 2023
AVANTAGE INLAY SIZE 50/28
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016
BD PLASTIPAK¿ 3ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 15, 2023
BD PLASTIPAK¿ 3ML SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 18, 2023
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
AVANTAGE E1 INSERT DIA28 S56
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·July 21, 2016
UNKNOWN BIOMET AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017
G7 BISPHERICAL SHELL 50D
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·December 15, 2025
AVANTAGE INSERT
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LPH·June 2, 2017
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·May 9, 2013
ACCU-CHEK ® RAPID-D INFUSION SET
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FPA·September 23, 2014
ZOOM CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 18, 2011