1,895 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BLADDERSCAN
FDA Adverse Event
Malfunction
·VERATHON·Product code EXQ·March 11, 2010
BLADDERSCAN
FDA Adverse Event
Malfunction
·VERATHON·Product code EXQ·March 11, 2010
BVI9400
FDA Adverse Event
VERATHON·Product code EXQ·March 11, 2010
BLADDERSCAN BVI 3000
FDA Adverse Event
Malfunction
·VERATHON INC.·Product code EXQ·June 1, 2010
BVI 3000 DOME PROBE ASSY
FDA Adverse Event
Malfunction
·VERATHON MEDICAL·Product code EXQ·February 15, 2013
BVI 3000 DOME PROBE ASSY
FDA Adverse Event
Malfunction
·VERATHNO MEDICAL·Product code EXQ·February 15, 2013
BVI 3000 CONTROL BOX
FDA Adverse Event
Malfunction
·VERATHON MEDICAL·Product code EXQ·February 15, 2013
BVI 3000 CONTROL BOX
FDA Adverse Event
Malfunction
·VERATHON MEDICAL·Product code EXQ·February 15, 2013
PUMP ON THE URODYNAMIC STUDY SYSTEM - UDS
FDA Adverse Event
Malfunction
·LABORIE MEDICAL TECHNOLOGIES CORP.·Product code EXQ·December 26, 2024
Laborie Medical Technologies Urodynamic Catheters, Twin Lumen 6 Fr , 40cm For Cystometry. Catalog Number: CAT-206.
FDA Recall
Terminated
·Laborie Medical Technologies Cor·Product code EXQ·April 9, 2009
Cystometer, Electrical Recording
FDA classification
FDA Class 2
·Cystometer, Electrical Recording
Exo Works
FDA UDI
Exo Imaging, Inc.·00850018318013·
Exo Iris
FDA UDI
Exo Imaging, Inc.·00850018318006·Exo Iris is a hand-held, general-purpose diagno...
Exo Iris Ultrasound System
FDA UDI
Exo Imaging, Inc.·00850018318068·Exo Iris Ultrasound System is a procedural pack...
Snakestaff Systems
FDA UDI
Snakestaff Systems, LLC·00860010714805·Everyday Carry Tourniquet (ETQ) - Gen 1 - 1.0" ...
Exo-s Saint-Damien Inc.
FDA registration
Exo-s Saint-Damien Inc.·1 product·🇨🇦 Canada
TRACKER
FDA UDI
GS Medical Co., Ltd.·08806162110944·Expander
ELECTRO-IMMUNO-QUANTITATION (EIQ)
FDA 510(k)
FDA Class 2
·Immunology
ultrasonic transducer
FDA UDI
Edan Instruments, Inc.·06944413805842·
ultrasonic transducer
FDA UDI
Edan Instruments, Inc.·06944413806702·