7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Protective Cap
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668103142·BINDER LASIK FLAP ELEVATOR
BD ECLIPSE BIFURCATED NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
E-PICCO CONTINUOUS CARDIAC OUTPUT MODULE AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Cardiovascular
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011
GYNECARE PROLIFT +M POSTERIOR PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 18, 2013