28 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANECARE LLC
FDA registration
ANECARE LLC·2 products·🇺🇸 United States
ANEclear
FDA UDI
ANECARE, LLC·00863034000329·Anesthesia Recovery Device
BALLARD CLOSED SUCTION SYSTEM
FDA Adverse Event
Injury
·AVANOS MEDICAL INC.·Product code BSY·July 10, 2025
LUXSTAR TRACK MOUNT LIGHT
FDA Adverse Event
Malfunction
·DENTAL EQUIPMENT, LLC (DBA NEWBERG MFG)·Product code EAZ·February 23, 2012
LUXSTAR POST MOUNT LIGHT
FDA Adverse Event
Malfunction
·DENTAL EQUIPMENT LLC (DBA NEWBERG MANUFACTURING·Product code EAZ·January 28, 2012
LUXSTAR UNIT-MOUNT LIGHT
FDA Adverse Event
Malfunction
·DENTAL EQUIPMENT LLC (DBA NEWBERG MFG)·Product code EAZ·July 19, 2011
LUXSTAR UNIT MOUNT LIGHT
FDA Adverse Event
Malfunction
·DENTAL EQUIPMENT LLC (DBA NEWBERG MANUFACTURING)·Product code EAZ·October 17, 2011
MAXSTAR ORBIT UNIT MOUNT LIGHT
FDA Adverse Event
Malfunction
·DCI EQUIPMENT·Product code EAZ·July 11, 2012
MAXSTAR UNIT-MOUNT LIGHT
FDA Adverse Event
Malfunction
·DENTAL EQUIPMENT LLC (DBA NEWBERG MANUFACTURING)·Product code EAZ·October 5, 2011
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
VOLISTA STANDOP
FDA Adverse Event
Malfunction
·MAQUET SAS·Product code FSY·March 19, 2019
LUXSTAR STANDARD UNIT MOUNT LIGHT
FDA Adverse Event
Malfunction
·MARUS·Product code EAZ·June 11, 2013
MAXSTAR UNIT MOUNT LIGHT
FDA Adverse Event
Malfunction
·MARUS·Product code EAZ·January 16, 2013
MAXSTAR CEILING MOUNT LIGHT
FDA Adverse Event
Malfunction
·MARUS·Product code EAZ·February 28, 2013
LUXSTAR CEILING MOUNT LIGHT
FDA Adverse Event
Injury
·MARUS·Product code EAZ·August 14, 2013