33 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Painmaster
FDA UDI
Painmaster·00781604000138·Bell Shaped Snap Tens Electrode- 20x90mm in Size
Painmaster
FDA UDI
Painmaster·00781604000121·Women's Oval Snap Tens Electrode - 40x90mm in Size
Painmaster MCT Patch
FDA 510(k)
FDA Class 2
·Neurology
PAINMASTER MCT PATCH
FDA 510(k)
FDA Class 2
·Neurology
PAINMASTER MCT PATCH
FDA 510(k)
FDA Class 2
·Neurology
STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·September 25, 2020
NEWMARK PAINMASTER MCT PATCH
FDA Adverse Event
Other
·NEWMARK, INC.·Product code LBF·November 10, 2009
SILASTIC(R) MAMMARY IMPLANT
FDA Adverse Event
Injury
·DOW CORNING CORP·Product code FTR·November 25, 1996
UNK MAMMARY IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·September 13, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·December 18, 2017
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 1, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·June 28, 2016
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·February 12, 2020
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·May 4, 2018
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·October 17, 2019
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·October 17, 2019
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·July 16, 2019
PUMP IN STYLE BREAST PUMP
FDA Adverse Event
Injury
·MEDELA, INC.·Product code HGX·August 11, 2011
MAXILIFT
FDA Adverse Event
Malfunction
·ARJO MED AB LTD.·Product code FNG·July 16, 2008
MULTIRATE INFUSOR SV; MULTIRATE INFUSER LV; BAXTER PAIN MATE PAIN MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital