17 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Celesteion, PCA-9000A/3, V6.5
FDA 510(k)
FDA Class 2
·Radiology
NON-STERILE, POWDER FREE BLACK NITRILE EXAMINATION GLOVES WITH CHERRY FLAVOR
FDA 510(k)
FDA Class 1
·General Hospital
ASPIRE CR FOR MAMMOGRAPHY SYSTEM (CRM); FCR ASPIRE CRN (READER). NOTE FOR GENERAL RADIOGRAPHY, READER IS CARBON XL2/FCR
FDA 510(k)
FDA Class 2
·Radiology
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·August 17, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·May 21, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·August 12, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·July 8, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·July 8, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·June 26, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·July 8, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·August 19, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CBK·July 15, 2020
TRILOGY EVO
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·July 24, 2020
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code CBK·July 7, 2020
LAUREATE WORLD PHACO SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 14, 2013
VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code LFX·July 27, 2011
PLUM 1.6 PUMP
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·September 30, 2008