17 results
·
23ms
·
Sources: EU EUDAMED, US FDA
AXIOS Stent with Electrocautery Enhanced Delivery System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 19, 2025
AXIOS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 17, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·February 20, 2025
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·December 18, 2024
AXIOS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 27, 2024
Oticon
FDA UDI
Oticon A/S·05707131280442·NERA2 PRO, BTE 13 WL 85 CNB
GUTTA PERCHA POINTS
FDA UDI
DiaDent Group International·08806383507394·Gutta Percha Points is used to root canal filin...
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171027867·PESSARY, CUBE #10, W/O DRAINS, 75mm
FLXIS
FDA 510(k)
FDA Class 2
·Radiology
DIGITAL SPOT MAMMOGRAPHY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BD POSIFLUSH¿ SF SALINE SYRINGE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND CO.·Product code NGT·September 19, 2018
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014
M2A 38MM MODULAR HEAD -6MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 6, 2013
NI
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KWP·June 24, 2011