25 results · 24ms · Sources: EU EUDAMED, US FDA

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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