8 results
·
34ms
·
Sources: EU EUDAMED, US FDA
STERILE .9% SODIUM CHLORIDE SOLUTION
FDA 510(k)
FDA Class 2
·General Hospital
NobelZygoma TiUltra Implant system
FDA 510(k)
FDA Class 2
·Dental
BACTERIURIA DETECT. DEVICE APTEK II
FDA 510(k)
FDA Class 1
·Microbiology
HL20 BUBBLE SENSOR
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTQ·January 30, 2015
TAPERLOC COMPLETE PRIMARY STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·May 7, 2024
ALARIS PUMP MODULE
FDA Adverse Event
Injury
·CAREFUSION CORP.·Product code FRN·January 30, 2013
MEDIAL LISFRANC PLATE - UNKNOWN
FDA Adverse Event
Other
·NEWDEAL·Product code HRS·December 21, 2010
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
JUMAO MEDICAL EQUIPMENT·Product code IOR·July 18, 2014