9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
QUICK-SERTER, MODEL 395
FDA 510(k)
FDA Class 2
·General Hospital
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111031·INSTRUMENT CADDY LARGE
Stainless Steel
FDA UDI
Seaspine Orthopedics Corporation·10889981114855·Sterilization Case, Deformity Pedicle Screws
Astraguard
FDA UDI
S D I DIAGNOSTICS INC·B279S297992300·Bacterial viral filter
MODIFICATION TO D3 ULTRA DFA RESPIRATORY VIRUS SCREENING & ID KIT
FDA 510(k)
FDA Class 1
·Microbiology
EnlightenVue Microendoscopy System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ISOLINE
FDA Adverse Event
Injury
·SORIN CRM·Product code MRM·March 1, 2013
SPRINT QUATTRO SECURE S
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011
CONSULTA CRT-D
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014