34 results · 22ms · Sources: EU EUDAMED, US FDA

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SILS PORT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

FlexStep

FDA UDI
Liftup A/S·05714420032538·FlexStep V2, 900, 6 step, outdoor

Laparoscope

FDA UDI
SOPRO-COMEG GmbH·04059082032238·

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172970126·

HISONIC-TRD TINNITUS RELIEF DEVICE

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

BIOMET'S MINIMALLY CONSTRAINED ELBOW

FDA 510(k)
FDA Class 2 ·Orthopedic

PLATE, FIXATION, BONE

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

NC TREK CORONARY DILATATION CATHETER

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code LOX·December 16, 2022

VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWC·June 18, 2013

ILAB ULTRASOUND IMAGING SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - FREMONT (CE)·Product code OBJ·May 9, 2013

INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·September 19, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 25, 2011

VA LOCKSCR Ø2.7 HEAD 2.4 SELF-TAP L14 TA

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWC·April 27, 2022

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

MIC PERCUTANEOUS ENDOSCOPIC GASTROSTOMY PEG KIT WITH ENFIT CONNECTORS - 20 FR

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code KNT·October 29, 2021

SCREW,FIXATION,BONE

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code HWC·December 30, 2014

UNK - SCREWS: 2.7 MM VA LOCKING

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWC·March 1, 2024

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·July 22, 2016

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·August 12, 2016

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·October 24, 2015