34 results
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69ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DESIGN STANDARDS CORP.
FDA registration
DESIGN STANDARDS CORP.·20 products·🇺🇸 United States
VBAS Extension Arm
FDA UDI
DESIGN STANDARDS CORP.·00850003228075·Extension arm for use with the VYCOR Brain Acce...
SKIN STAPLER
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP.·Product code GDT·October 10, 2019
SKIN STAPLER
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP.·Product code GDT·August 27, 2020
CTS RELIEF KIT 4 EA
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code MDM·August 30, 2021
PERMACLIP REEUSABLE HANDLE W/DISP. CLIP CART.
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP·Product code FZP·July 25, 2008
PERMACLIP REUSABLE HANDLE W/DISP. CLIP
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP·Product code GDO·July 25, 2008
PERMACLIP DISPOSABLE CARTRIDGE, 10MM CLIPS
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP·Product code FZP·July 25, 2008
PERMACLIP DISPOSABLE CARTRIDGE, 10MM CLIPS
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code FZP·July 30, 2008
PERMACLIP REUSABLE HANDLE W/DISP. CLIP CART
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code GDO·July 30, 2008
PERMACLIP REUSABLE HANDLE W/DISP. CLIP CART
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code FZP·July 30, 2008
CARPEL TUNNEL SYNDROME (CTS) RELIEF KIT
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code MDM·March 26, 2021
CARPEL TUNNEL SYNDROME (CTS) RELIEF KIT
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code MDM·January 19, 2021
CARPEL TUNNEL SYNDROME (CTS) RELIEF KIT
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code MDM·January 14, 2021
PERMACLIP REUSABLE HDL. W/DISP. CLIP CARTRIDGE
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP·Product code GDO·January 4, 2008
PERMACLIP DISPOSABLE CARTRIDGE 10MM CLIPS
FDA Adverse Event
Injury
·DESIGN STANDARDS CORP·Product code GDO·March 13, 2008
PERMACLIP REUSABLE HD1. W/DISP.CLIP CARTRIDGE
FDA Adverse Event
Malfunction
·DESIGN STANDARDS CORP·Product code GDO·January 4, 2008
LIFESYNC LEADWEAR
FDA Adverse Event
Other
·LIFESYNC CORPORATION·Product code DSA·January 9, 2009
MITROFLOW AORTIC PERICARDIAL HEART VALVE
FDA Adverse Event
Injury
·LIVANOVA CANADA CORP.·Product code DYE·October 28, 2016
GN RESOUND
FDA Adverse Event
Injury
·GN HEARING A/S·Product code OSM·September 21, 2022