96 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ARIATELE TELEMETRY TRANSMITTER (96281)
FDA 510(k)
FDA Class 2
·Cardiovascular
Micro Finger and Spatula
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896103030·Micro Finger and Spatula Double Ended Right Han...
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515234499·Shepard Bipolar Fcps, str
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613052485·Cushing Bayonet Bipolar Forcep 7 1/2" (190.5mm)...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613069018·Cushing Bayonet Bipolar Forcep 7 1/2" (190.5mm)...
MAXIFLEX - SEMI FLEX SCOPE, 25 TO 65 CM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
EXTENSION SET LIGHT-SAFE, MODEL BC565
FDA 510(k)
FDA Class 2
·General Hospital
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·August 4, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·August 4, 2017
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FCG·January 3, 2017
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Malfunction
·COOK IRELAND LTD·Product code FGE·February 2, 2016
EVOLUTION® BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·September 27, 2016
FGE CATHETER, BILIARY, DIAGNOSTIC - BILIARY STENT - METAL
FDA Adverse Event
Injury
·COOK INC·Product code FGE·January 29, 2020
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 31, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 30, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·March 30, 2019
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013
FLEXI-SEAL FECAL MANAGEMENT SYSTME KIT
FDA Adverse Event
Malfunction
·CONVATEC, INC.·Product code KNT·July 29, 2014