38 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Myriad Particles
FDA 510(k)
FDA Unclassified
·Unknown
ReLine
FDA UDI
Nuvasive, Inc.·00195377047410·RELINE-O Trial, 6mm H Offset Left L-pop
PureLife X-Ray Film
FDA UDI
Flow X Ray Corporation·00812045030740·PLD-57 Size 2 Double
VIVA XT
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·April 11, 2014
OsteoMed
FDA UDI
OSTEOMED LLC·00845694053730·M4 Mini Plate Organizer
IRIS SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055162·IRIS SCISSORS STRAIGHT TUNGSTEN CARBIDE BLADES ...
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869605007·MOSS 100 Approximator
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869611749·MOSS Hook/Connector Approximator
SOLO ORTHO 3
FDA 510(k)
FDA Class 2
·Dental
STEAM/EO RECORD CARD, MODEL CI 121
FDA 510(k)
FDA Class 2
·General Hospital
MICROSCAN RAPID POS INOCULUM BROTH
FDA Adverse Event
Malfunction
·DADE BEHRING, INC.·Product code JSO·August 13, 2005
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Injury
·TANDEM DIABETES CARE·Product code QFG·September 27, 2021
SPRINT
FDA Adverse Event
Injury
·MPRI·Product code LWS·June 8, 2018
BD FILTER NEEDLE 19G X 1/2 IN
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·October 22, 2020
HEART LUNG MACHINE
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY GMBH·Product code KFM·February 20, 2025
BACT/ALERT FN CULTURE BOTTLES
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code JTA·December 21, 2007
VIRTUOSO DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 10, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 24, 2014
UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code DHA·August 11, 2011
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 1, 2013