10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CHEMO-PORT
FDA 510(k)
FDA Class 2
·General Hospital
Wrist Electronic Sphygmomanometer
FDA 510(k)
FDA Class 2
·Cardiovascular
Titan Manufacturing Bipolar Forceps
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REUSABLE NEONATAL SINGLE HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 9, 2017
BD VACUTAINER® SINGLE USE HOLDER
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·December 6, 2017
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 14, 2014
POWER PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·January 14, 2013
SPRINT QUATTRO SECURE S
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 3, 2010
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·October 15, 2025
REUSABLE NEONATAL SINGLE HEATED BREATHING CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 23, 2023