15 results · 27ms · Sources: EU EUDAMED, US FDA

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DAIG ELECTROPHYSIOLOGY CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

Snowden-Pencer

FDA UDI
STERIS CORPORATION·10885403181757·DIAMOND-FLEX 90 DEG ARTICULATING FORCEPS BABCOC...

InFix®

FDA UDI
ZIMMER SPINE, INC.·00889024332058·

SOLUTION TRANSFER SET

FDA 510(k)
FDA Class 2 ·General Hospital

TITERTEK MICROPLATE WASHER 120

FDA 510(k)
FDA Class 1 ·Microbiology

LONG NAIL KIT R2.0, TI, LEFT GAMMA3 ?11X400MM X 13

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 4, 2012

1.5MM SYSTEM TWIST DRILL WITH J NOTCH 1.1 X 50MM, 9MM STOP

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·June 17, 2020

TW DRILL 1.1X50MM 9MMSTOP W/NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·May 5, 2021

TW DRILL 1.1X50MM 9MMSTOP W/NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·February 17, 2021

PROMUS ELEMENT ?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 25, 2014

VANGUARD PS TIBIAL TRIAL POST

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code IQO·November 9, 2010

MANTIS CANNULATED POLYAXIAL SCREW 7.5 X 40 MM

FDA Adverse Event
Malfunction ·STRYKER SPINE BORDEAUX·Product code MNH·December 27, 2012

TW DRILL 1.1X50MM 9MMSTOP W/NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·November 29, 2021

TW DRILL 1.1X50MM 9MMSTOP W/NT

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HBE·May 5, 2021

LACTOSORB SYSTEM 1.5MM ADJUSTABLE SELF-DRILLING TAP

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HWX·June 17, 2020