15 results
·
34ms
·
Sources: EU EUDAMED, US FDA
ENDOMEDIX Y-ADAPTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SeaSpine Spacer System - Hollywood
FDA UDI
Seaspine Orthopedics Corporation·10889981090012·Hollywood Angled Inserter
PCA (R) TIBIAL BONE WEDGES
FDA 510(k)
FDA Class 2
·Orthopedic
OP-CON SURG. INSTRUMENT #10
FDA 510(k)
FDA Class 1
·Neurology
CHAMBER COMPLETE AUTOFEED 900
FDA Adverse Event
Malfunction
·Product code BTT·May 5, 2021
CHAMBER COMPLETE AUTOFEED 900
FDA Adverse Event
Malfunction
·Product code BTT·January 21, 2020
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013
NEXGEN MIS TOTAL STEMMED TIBIAL COMPONENT
FDA Adverse Event
Malfunction
·ZIMMER INC·Product code JWH·December 8, 2010
NATURALYTE
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014
VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 17, 2023
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 20, 2023
VENTED AUTOFEED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 23, 2024
CHAMBER COMPLETE AUTOFEED 900
FDA Adverse Event
Malfunction
·Product code BTT·June 3, 2021
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 15, 2024
CHAMBER COMPLETE AUTOFEED 900
FDA Adverse Event
Malfunction
·Product code BTT·February 4, 2021