10,000 results
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71ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NHS INC
FDA registration
NHS INC·1 product·🇺🇸 United States
NHS 2009SP HEARING AID
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ALARA Neuro Access Needle Kit
FDA UDI
SURGENTEC, LLC·00858406007334·ALARA Neuro Access Needle Kit with Extension Ha...
ALARA Neuro Access Needle Kit
FDA UDI
SURGENTEC, LLC·00858406007341·ALARA Neuro Access Needle Kit with Extension Ha...
NHS 2044P BODY AID, HEARING AID
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
NHS Scotland Cataract Set Rayner 74
FDA UDI
Hasa Optix·05404027449470·
COAT-A-COUNT NHS-PROLACTIN KIT AND
FDA 510(k)
FDA Class 1
·Clinical Chemistry
UNK GEL BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·August 13, 2023
NAIL HOLDING SCREW GAMMA3® 8X35MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·July 12, 2017
NAIL HOLDING SCREW GAMMA3® 8X35MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·December 17, 2015
TARGET DEVICE GAMMA3® 300X160MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code HSB·December 17, 2015
NAIL HOLDING SCREW GAMMA3 8X35MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS-KIEL·Product code LXH·April 12, 2013
NAIL HANDLE T2 TIBIA
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·July 22, 2014
NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·July 22, 2014
NAIL HANDLE T2 TIBIA
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·July 11, 2016
NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·July 11, 2016
NAIL HOLDING SCREW GAMMA3® 8X35MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·September 26, 2016
SPEEDLOCK SLEEVE GAMMA3® 180
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·June 23, 2016
NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM
FDA Adverse Event
Malfunction
·STRYKER TRAUMA KIEL·Product code LXH·June 27, 2016
6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE, OUS
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code MGB·September 17, 2023