14 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Digital Wireless Intraoral X-Ray Sensor
FDA 510(k)
FDA Class 2
·Dental
Oticon
FDA UDI
Sbo Hearing A/S·05714464032884·More 2 FW 1.1.0
BD BBL™ Sensi-Disc™ Tetracycline 30 µg
FDA UDI
BECTON, DICKINSON AND COMPANY·00382902309987·BD BBL™ Sensi-Disc™ Tetracycline 30 µg
BD POSIFLUSH PRE-FILLED SALINE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·March 19, 2018
SYNGO.VIA WEB VIEWER
FDA 510(k)
FDA Class 2
·Radiology
MEDRELIEF SE SERIES, MODELS SE-50, SE-100, SE-200, SE-300
FDA 510(k)
FDA Class 2
·Physical Medicine
BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998 and 231344¿
FDA Enforcement
Class II
·Ongoing·Becton Dickinson & Co.·February 14, 2024
RAPID EXCHANGE BILIARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code FGE·October 28, 2008
ADJUSTABLE WIRE COLLET
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·July 19, 2011
GYNECARE PROLIFT +M ANTERIOR PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 17, 2013
KIWI VACUUM ASSISTED DELIVERY SYSTEM
FDA Adverse Event
Injury
·CLINICAL INNOVATIONS, LLC·Product code HDB·April 3, 2024
KIWI VACUUM ASSISTED DELIVERY SYSTEM
FDA Adverse Event
Injury
·CLINICAL INNOVATIONS, LLC·Product code HDB·April 3, 2024
BD POSIFLUSH¿ SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·March 15, 2018
BD BBL Sensi Disc Tetracycline 30 ug,used for semi-quantitative in vitro susceptibility testing. Catalog Number 230998 and 231344
FDA Recall
Open, Classified
·Becton Dickinson & Co.·Product code JTN·January 8, 2024