11 results
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41ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MARC PRO, INC.
FDA registration
MARC PRO, INC.·2 products·🇺🇸 United States
Marc Pro, Inc
FDA UDI
MARC PRO·00854784005016·
Marc Pro
FDA UDI
MARC PRO·00854784005009·Powered Muscle Stimulator
Marc Pro, Inc
FDA UDI
MARC PRO·00854784005023·Electrode, Cutaneous
GUARDIAN
FDA Adverse Event
(MARS PRO)·Product code IKX·August 31, 2006
KOH MARCRO NEEDLE HOLDER
FDA Adverse Event
Injury
·KARL STORZ SE & CO. KG·Product code GCJ·July 8, 2022
PLUM XL3M MICRO/MARCRO PUMP
FDA Adverse Event
Injury
·HOSPIRA, INC.·Product code FRN·May 18, 2005
PLUM XL3M MICRO/MARCRO PUMP
FDA Adverse Event
Death
·HOSPIRA, INC.·Product code FRN·August 10, 2004
GUARDIAN
FDA Adverse Event
Injury
·JAN MAO (MARS PRO)·Product code KNN·April 5, 2006
GUARDIAN
FDA Adverse Event
Other
·JAN MAO (MARS PRO)·Product code FSA·March 21, 2005
BKP CEMENT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·February 24, 2023