13 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FLEXIBLE FIBERSCOPES AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79804011·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79804010051·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79804010101·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79804011001·Sprint II Bracket McLaugh/Benn/Trev. .022" max....
Disposable Cuff
FDA UDI
SUNTECH MEDICAL, INC.·10840935103714·
TiWAVE-C Porous Titanium Cervical Cage
FDA 510(k)
FDA Class 2
·Orthopedic
SHELL CAGE, WAVE CAGE, LOOP CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
SAFE MICRO HOLLOW FIBRE OXYGENATOR
FDA Adverse Event
Malfunction
·POLYSTAN A/S·Product code DTZ·April 29, 1998
3.5MM TI LCP® METAPHYSEAL PLATE 12 HOLES
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXT·August 22, 2019
2008K HEMODIALYSIS SYSTEM
FDA Adverse Event
Death
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·June 25, 2014
2520274-2013-10530
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MNI·February 22, 2013
CRRT
FDA Adverse Event
Malfunction
·GAMBRO·Product code KDI·January 29, 2011