7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BENTLEY MANUALLY OPERATED WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
artegral
FDA UDI
Merz Dental GmbH·D7091970311·anteriors; shade C2; mould UCS
Reprocessed Agilis NxT Steerable Introducer
FDA 510(k)
FDA Class 2
·Cardiovascular
CARDIOBLATE GEMINI SURGICAL ABLATION DEVICE, MODELS 49260 AND 49261
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROXIMATE** LINEAR CUTTER RELOAD - STANDARD
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·February 20, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 31, 2014
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 14, 2011