8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TYMPANOSTOMY TUBE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981575·anteriors; shade A3 light; mould BM6
HU/HS/HG PROSTHETIC SYSTEM
FDA 510(k)
FDA Class 2
·Dental
DISPOSABLE LYMPHANGIOGRAM SET
FDA 510(k)
FDA Class 2
·General Hospital
OPTI-FREE PLUS
FDA Adverse Event
Injury
·ALCON LABORATORIES, INC.·Product code LPN·December 12, 2017
PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·February 27, 2013
STENOSCOP
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVIATE LTD.·Product code JAA·January 31, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 5, 2014