7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AERO-MIST NEBULIZER HEATER
FDA 510(k)
FDA Class 2
·Anesthesiology
ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DR
FDA 510(k)
FDA Class 2
·Radiology
EMBRYOASSIST AND EMBRYOASSIST WITH PHENOL RED
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 19, 2012
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 30, 2014
PUMP IN STYLE BREASTPUMP SHOULDER BAG
FDA Adverse Event
Other
·MEDELA, INC.·Product code HGX·October 13, 2010
Segmental Stem, Canal Filling, Bowed 152MM, 1 EACH. Model Numbers: FB-11152-03M, FB-12152-03M, FB-13152-03M, FB-14152-03M, FB-15152-03M, FB-16152-03M, FB-17152-03M, FB-18152-03M, FB-19152-03M, FB-20152-03M, FB-21152-03M. Component of ELEOS LIMB SALVAGE SYSTEM
FDA Enforcement
Class II
·Ongoing·Onkos Surgical, Inc.·June 4, 2025