11 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EzDent-i / E2 / Prora View
FDA 510(k)
FDA Class 2
·Radiology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690127291·Apex Revision Knee System-Revision Femur Size 1...
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306821806·Laryngeal Mirror #7
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101070·WALTON CONJUNCTIVA RETRACTOR
CORIN TRINITY ACETBULAR SYSTEM WITH HXLPE LINERS
FDA 510(k)
FDA Class 2
·Orthopedic
MRIDIUM 3860 MRI INFUSION PUMP/MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
CONCERTO, BASIC & SHOWER TROLLEY
FDA Adverse Event
Other
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·March 1, 2011
MCLEAN-RING NASOJEJUNAL FEEDING TUBE SET
FDA Adverse Event
Injury
·COOK INC·Product code KNT·November 10, 2021
AFFINITY DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code DXY·January 11, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013
SELOX SR 53
FDA Adverse Event
Malfunction
·BIOTRONIK, SE & CO KG·Product code NVZ·June 29, 2011