10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Microlife Digital Infrared Forehead Thermometer, Model FR1MN1-1
FDA 510(k)
FDA Class 2
·General Hospital
Deploy™ Expandable Interbody System
FDA UDI
Southern Spine LLC·00815351022621·Lumbar Expandable Cage, 16 Degree, 28mm Length,...
FOCUS (TM) ECHOGENIC NERVE STIMULATING NEEDLE
FDA 510(k)
FDA Class 2
·Anesthesiology
EMV3 SELF MONITORING BLOOD GLUCOSE SYSTEM, EMV3 PRO SELF MONITORING BLOOD GLUCOSE SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CAPSUREFIX MRI SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC SINGAPORE OPERATIONS·Product code NVN·October 10, 2014
SOVEREIGN
FDA Adverse Event
Injury
·ABBOTT MEDICAL OPTICS (AMO)·Product code HQC·July 8, 2011
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 3, 2013
LUCAS 3 CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024
LUCAS 3 CHEST COMPRESSION SYSTEM
FDA Adverse Event
Death
·JOLIFE AB - 3005445717·Product code DRM·February 6, 2024
BIO-COMPOSITE SWIVELOCK
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MAI·June 3, 2016