25 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
miniARM® multiSTATION™ System
FDA UDI
LSI Solutions, Inc.·00850200006919·miniARM® ACCESS ADAPTER
Actera hip system
FDA UDI
Conformis, Inc.·00810933031398·Actera Stem Acetate -120% Magnification Template
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014606903·GETINGE / SHAMPAINE 4900/5100B, 5100E 5.25" DE...
PICCOLO CHLORIDE TEST SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
NITRILE EXAM GLOVE, POWDER FREE, BLUE
FDA 510(k)
FDA Class 1
·General Hospital
UNKNOWN MILLER-GALANTE KNEE IMPLANT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
UNKNOWN MILLER-GALENTE KNEE IMPLANT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
UNKNOWN MILLER-GALANTE KNEE IMPLANT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
UNKNOWN MILLER-GALANTE KNEE IMPLANT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
UNKNOWN MILLER-GALANTE ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
UNKNOWN MILLER-GALANTE ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
UNKNOWN MILLER-GALANTE ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 23, 2015
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009
ENTERPRISE 8000
FDA Adverse Event
Injury
·ARJOHUNTLEIGH POLSKA SP. ZO.O.·Product code FNL·April 8, 2013
ENDEAVOR RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·April 26, 2011
DA VINCI S SURGICAL SYSTEM
FDA Adverse Event
Other
·INTUITIVE SURGICAL, INC.·Product code NAY·July 21, 2008
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009