26 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PENRITH ELETTRA ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
EXTRACTING FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896081802·EXTRACTING FORCEPS TUNGSTEN CARBIDE DUST TIPS #32
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450585306·
HS Diam. Burr, Ø4.0x150, 80k
FDA UDI
Bien-Air Surgery SA·17630055507393·
BAXANO IO-FLEX SYSTEM
FDA Adverse Event
Other
·BAXANO, INC.·Product code HAE·July 2, 2012
BAXANO IO-FLEX SYSTEM
FDA Adverse Event
Other
·BAXANO, INC.·Product code HAE·July 2, 2012
SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL
FDA 510(k)
FDA Class 2
·Hematology
5F GUIDING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BAXANO IO-FLEX SYSTEM
FDA Adverse Event
Other
·BAXANO, INC.·Product code HAE·July 2, 2012
QUANTA SYSTEM S.P.A.
FDA Adverse Event
Malfunction
·QUANTA SYSTEM, S.P.A.·Product code GEX·December 21, 2012
VANGRD PS BOX REAMER 62.5-67.5
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HTO·May 8, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 19, 2014
UNKNOWN DEPUY AGILITY SZ 5 INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HSN·May 17, 2011
M2A 1 PC SHELL 38MMX50MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 23, 2013
LAT CLAW CONNECTOR 40/50MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·October 23, 2013
REACH 11X200 100% POR FMRL STR
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·May 2, 2014
M2A 38MM MOD HD STD NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 2, 2014
M2A 1 PC SHELL 38MMX50MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 2, 2014
FREEDOM STD FACE LINER SZ 24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWZ·October 23, 2013
ARCOMXL 36MM RLC LINER HW SZ24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LZO·October 23, 2013