10,000 results
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49ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909040CFGK1·NTI Diamond Coarse FG
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909037MFGK1·NTI Diamond Medium FG
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909037SCFGK1·NTI Diamond SuperCoarse FG
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909040MFGK1·NTI Diamond Medium FG
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909040SCFGK1·NTI Diamond SuperCoarse FG
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909037CFGK1·NTI Diamond Coarse FG
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909040CFGK3·NTI Gold Pack (2x25) 909-040-C
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909040SCFGK3·NTI Gold Pack (2x25) 909-040-SC
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310909040FFGK1·NTI Diamond Fine FG
LITHOTRITE
FDA Adverse Event
Other
·KARL STORZ GMBH & CO.·Product code FGK·April 26, 1996
LITHOTRIPTOR
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUMENTS INC.·Product code FGK·January 6, 1994
KARL STORZ
FDA Adverse Event
Malfunction
·KARL STORZ·Product code FGK·July 7, 1997
STORZ
FDA Adverse Event
Injury
·KARL STORZ ENDOSCOPY-AMERICA INC.·Product code FGK·June 23, 1997
STORZ
FDA Adverse Event
Malfunction
·STORZ·Product code FGK·November 26, 1996
KARL STORZ ENDOSCOPY
FDA Adverse Event
Malfunction
·KARL STORZ ENDOSCOPY·Product code FGK·October 30, 2007
OLYMPUS LITHOTRIPSER BASKET
FDA Adverse Event
Malfunction
·OLYMPUS CORPORATION·Product code FGK·August 2, 1993
LITHOTRITE
FDA Adverse Event
Malfunction
·KARL STORZ ENDOSCOPY-AMERICA INC·Product code FGK·October 16, 1997
Tripsor, Stone, Bladder
FDA classification
FDA Class 2
·Tripsor, Stone, Bladder
FGX Canada Corp
FDA registration
FGX Canada Corp·2 products·🇨🇦 Canada
FKG DENTAIRE SARL
FDA registration
FKG DENTAIRE SARL·9 products·🇨🇭 Switzerland