10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
JIAJIAN ACUPUNCTURE NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036027711·
CORTEK MINI LAPAROSCOPE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PJUR EROS WATER FORMULATION
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
LUX 1440
FDA Adverse Event
Malfunction
·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012
ISODUR PROSTHESIS HEAD 12/14 32MM XL
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO KG·Product code LPH·March 28, 2014
VERCISE GENUS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·August 30, 2023
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 19, 2013
ISOMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·September 15, 2014
HOMECHOICE LOW RECIRCULATION VOLUME APD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 16, 2011