9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
COMPRESSION LEGGING DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704294293·
Patterson
FDA UDI
PATTERSON DENTAL SUPPLY, INC.·D6620708718891·FILE, PULP CANAL, ENDODONTIC
DATEX-OHMEDA S/5 CRITICAL CARE MONITOR WITH L-ICU05 AND L-ICU05A SOFTWARE
FDA 510(k)
FDA Class 2
·Cardiovascular
Reusable Blood Pressure Cuff
FDA 510(k)
FDA Class 2
·Cardiovascular
PRIMEADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 14, 2016
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 17, 2014
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 16, 2010
PRIMARY TRITANIUM HEMI CLUSTER HOLE CUP 60MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code LPH·December 6, 2012