7 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELECTRONIC SPIROMETER MODEL MFR-8100
FDA 510(k)
FDA Class 2
·Anesthesiology
DRYTOUCH SUCTION STIMULATOR PROBE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
DIALYSATE LINE WITH CONNECTORS/RE-USE WASH-OUT LINES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PU·Product code CBK·March 21, 2014
ENRHYTHM MRI
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code LWP·October 31, 2012
CVC SET: 3-LUMEN 7 FR X 20 CM
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code FOZ·June 1, 2015
Allura Xper FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025