10,000 results
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68ms
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Sources: EU EUDAMED, US FDA
MKJ BRANDS LLC
FDA registration
MKJ BRANDS LLC·4 products·🇺🇸 United States
Just for Us
FDA UDI
MKJ Brands Limited Liability Company·00855424008527·Just for Us™ Warming Jelly Water-based Personal...
Just for Her
FDA UDI
MKJ Brands Limited Liability Company·00855424008671·Just for Her™ Period Emergency Kit for Unexpect...
Just for Her
FDA UDI
MKJ Brands Limited Liability Company·00855424008985·Just for Her – Menstrual Pads, Regular, Unscented
Freshen-Up
FDA UDI
MKJ Brands Limited Liability Company·00855424008411·Freshen-Up Advanced Oral Care Toothbrush, 8 Pack
Just for Her
FDA UDI
MKJ Brands Limited Liability Company·00855424008978·Just for Her – Menstrual Pads, Super Long, Unsc...
Freshen-Up
FDA UDI
MKJ Brands Limited Liability Company·00855424008480·Freshen-Up Advanced Oral Care Medium Toothbrush...
Just for Her
FDA UDI
MKJ Brands Limited Liability Company·00855424008961·Menstrual Pads, Overnight, Unscented
MKJ
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 9, 2014
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRO·November 1, 2019
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRT·December 11, 2018
ACCESS CARDIO
FDA Adverse Event
Death
·ACCESS CARDIOSYSTEMS·Product code MVK·November 18, 2003
X SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRT·October 10, 2017
X SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRO·February 20, 2016
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRT·September 28, 2019
1220908-2016-00030
FDA Adverse Event
Malfunction
·January 21, 2016
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRO·July 18, 2019
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DPS·October 10, 2019
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRT·July 16, 2019
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code DRO·December 9, 2019