14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SNUGGLE WARM 4000 CONVECTIVE WARMING SYSTEM, MODEL SW4000
FDA 510(k)
FDA Class 2
·Cardiovascular
BUTTERFLY PLATE FUNCTION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
CADD
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·March 23, 2022
CADD MEDICATION CASSETTE
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·July 14, 2022
CADD
FDA Adverse Event
Malfunction
·NULL·Product code FPA·August 17, 2021
CADD MEDICATION CASSETTES
FDA Adverse Event
Malfunction
·ST PAUL·Product code FPA·June 6, 2022
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·April 8, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 22, 2011
GENICON SUCTION IRRIGATION SYSTEM
FDA Adverse Event
Malfunction
·GENICON·Product code GCX·May 7, 2008
BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·July 31, 2019
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·September 17, 2012
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
FDA Enforcement
Class II
·Terminated·Belmont Instrument Corporation·October 24, 2012
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
FDA Enforcement
Class II
·Terminated·Stryker Medical Division of Stryker Corporation·November 21, 2018