79 results · 23ms · Sources: EU EUDAMED, US FDA

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CYCLOSPORINE (CSA) FLEX REAGENT CARTRIDGE

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

AOS CANCELLOUS LOCKING SCREW 4.0mm x 65mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665008692·

OneTouch Ultra2

FDA UDI
LifeScan Europe GmbH·00353885010511·OneTouch Ultra2 Blood Glucose Monitoring System...

Arsenal

FDA UDI
ALPHATEC SPINE, INC.·00840967162379·OFFSET THORACIC SUPRALAMINAR HOOK, RIGHT, 6.5mm

3TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE

FDA 510(k)
FDA Class 1 ·Cardiovascular

SEEDNET, MODEL EP6T5, EP5E5

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HOMECHOICE, DOMESTIC 120V

FDA Adverse Event
BAXTER HEALTHCARE·Product code FKX·June 11, 2008

HOMECHOICE, DOMESTIC 120V

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·July 24, 2009

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

HOMECHOICE CYCLER-REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·December 4, 2007

HOMECHOICE CYCLER-REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·December 10, 2007

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 27, 2008

PD CYCLER 110 VOLT HOME CHOCIEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 18, 2008

HOMECHOICE CYCLER-REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 13, 2008

HOMECHOICE CYCLER -REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·June 5, 2008

HOMECHOICE CYCLER REFURBISHED

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE·Product code FKX·March 6, 2008

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 27, 2013

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 24, 2011