35 results
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54ms
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Sources: EU EUDAMED, US FDA
ASPIRE PRODUCTS, LLC
FDA registration
ASPIRE PRODUCTS, LLC·2 products·🇺🇸 United States
EMST150
FDA UDI
Aspire Products LLC·00793573085498·EMST150 expiratory muscle strength trainer (han...
EMST150 EXPIRATORY MUSCLE STRENGTH TRAINER
FDA Adverse Event
Injury
·ASPIRE PRODUCTS, LLC·Product code ION·September 3, 2024
BALLARD CLOSED SUCTION CATHETER, Y-ADAPTER, NEONATAL/PEDIATRIC
FDA Adverse Event
Malfunction
·AVENT S DE RL DE CV·Product code BSY·February 7, 2025
BALLARD CLOSED SUCTION SYSTEM
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code BSY·February 13, 2025
BALLARD CLOSED SUCTION SYSTEM FOR ADULTS
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code BSY·January 30, 2025
NEXUS® SONASTAR® SHORT HANDPIECE
FDA Adverse Event
Injury
·MISONIX, INC.·Product code LFL·May 3, 2024
BONESCALPEL® ULTRASONIC SURGICAL ASPIRATION SYSTEM
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·April 6, 2023
BALLARD CLOSED SUCTION CATHETER, Y-ADAPTER, NEONATAL/PEDIATRIC
FDA Adverse Event
Malfunction
·AVANOS MEDICAL INC.·Product code BSY·February 11, 2025
NEXUS® SONASTAR ELITE HANDPIECE
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·October 3, 2024
SONASTAR® ULTRASONIC SURGICAL ASPIRATION SYSTEM
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·December 23, 2022
NEXUS® STANDARD HANDPIECE
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·May 10, 2023
NEXUS® STANDARD HANDPIECE
FDA Adverse Event
Injury
·MISONIX, INC.·Product code LFL·July 18, 2023
SONASTAR® STANDARD LONG CURVED PROBE
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·March 21, 2024
NEXUS® ULTRASONIC SURGICAL ASPIRATOR SYSTEM
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·December 6, 2023
NEXUS® ULTRASONIC SURGICAL ASPIRATOR SYSTEM
FDA Adverse Event
Malfunction
·MISONIX, INC.·Product code LFL·December 6, 2023
Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to aspirate saliva, mucous, vomitus or other aspirant from the mouth or airway to allow adequate respiration or ventilation of the patient.
FDA Recall
Terminated
·Ohio Medical Corporation·Product code BTA·August 14, 2018
VIZIGO¿ SHEATH
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DYB·July 10, 2024
SMARTSITE 20MM VENTED VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code LHI·September 13, 2021
CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ SMALL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DYB·June 19, 2024