10,000 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LAUNCHER 6F GUIDE CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC, INC·Product code DQY·October 14, 2014
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·December 3, 2013
ALLIGATOR FORCEPS
FDA Adverse Event
Injury
·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code FJR·July 28, 1994
KLEPPINGER FORCEPS
FDA Adverse Event
RICHARD WOLF MEDICAL INSTRUMENT CORP.·Product code FJR·September 28, 1994
INTERSTIM NEUROSTIMULATOR, UNKNOWN
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·July 29, 2015
MULTI-LINK RX VISION CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code MAF·April 11, 2011
VOYAGER NC CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·August 16, 2011
Forceps, Disconnect
FDA classification
FDA Class 1
·Forceps, Disconnect
F4R
FDA UDI
NAKANISHI INC.·04560224971488·
F4R
FDA UDI
NAKANISHI INC.·04560264573734·
Faci Forms
FDA UDI
RELIANCE ORTHODONTIC PRODUCTS INC·D798FFR0·Faci Forms are intended for use as a mold for c...
AJR ENTERPRISES LLC
FDA registration
AJR ENTERPRISES LLC·6 products·🇺🇸 United States
FERRING PHARMACEUTICALS INC.
FDA registration
FERRING PHARMACEUTICALS INC.·1 product·🇺🇸 United States
AJR International S.R.L.
FDA registration
AJR International S.R.L.·2 products·🇩🇴 Dominican Republic
F.R. Thompson
FDA UDI
Howmedica Osteonics Corp.·07613327139679·Hip Endoprosthesis
F.R. Thompson
FDA UDI
Howmedica Osteonics Corp.·07613327139730·Hip Endoprosthesis
F.R. Thompson
FDA UDI
Howmedica Osteonics Corp.·07613327139785·Hip Endoprosthesis
F.R. Thompson
FDA UDI
Howmedica Osteonics Corp.·07613327139938·Hip Endoprosthesis
NAC-F4R
FDA UDI
NAKANISHI INC.·04560224982026·
F.R. Thompson
FDA UDI
Howmedica Osteonics Corp.·07613327139808·Hip Endoprosthesis