26 results · 26ms · Sources: EU EUDAMED, 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