83 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Q-SWITCHED ND:YAG LASER SYSTEM, MODEL GLOBALCURE-SC6
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741020500·
Essix A+®
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D74611020501·Essix A+® Plastic -.020in 125mm CIR
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0120500·Screwdriver, Assembled Screws SNI1
InSePtion MIS Fixation System
FDA UDI
Kalitec Direct LLC·B07314K0120500·Inserter, All-In-One
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674102050060·
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800039825856·Rod 5.5 x 50mm
Astra Spirometer
FDA UDI
S D I DIAGNOSTICS INC·B279S295102050·Spirometer
VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
R & D SYSTEMS XERET HEMATOLOGY CONTROL
FDA 510(k)
FDA Class 2
·Hematology
V200 / ESPRIT
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 16, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·March 28, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 19, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code CBK·May 20, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 7, 2021
V200 VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC·Product code CBK·December 9, 2020
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, LLC·Product code MNT·June 21, 2021
OPT BL VP V2 5MM STD W/FX
FDA Adverse Event
Malfunction
·COVIDIEN LP, FORMERLY US SURGICAL·Product code GCJ·April 22, 2013
MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·September 15, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011