174 results
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52ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MOSS TUBES, INC.
FDA registration
MOSS TUBES, INC.·2 products·🇺🇸 United States
Moss
FDA UDI
MOSS TUBES, INC.·00866459000400·Moss Gastrostomy Tube
Moss
FDA UDI
MOSS TUBES, INC.·00866459000417·Moss MarkIV Nasal Tube
MOSS TUBES, INC. NASAL TUBE - MARK IV
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MOSS GASTROSTOMY TUBE (5-17719)
FDA Adverse Event
Malfunction
·MOSS TUBES, INC.·Product code KNT·November 13, 2015
MOSS GASTROSTOMY TUBE (5-17719)
FDA Adverse Event
Death
·MOSS TUBES, INC.·Product code KNT·November 4, 2015
MOSS TRANSGASTRIC JEJUNAL FEEDING TUBE
FDA Adverse Event
Malfunction
·MOSS TUBES, INC.·Product code KNT·March 10, 2008
MOSS MARK IV NASAL TUBE
FDA Adverse Event
Other
·MOSS TUBES, INC.·Product code BSS·May 10, 2007
MOSS
FDA Adverse Event
Injury
·MOSS TUBES, INC.·Product code KNT·January 8, 2010
MOSS GASTROSTOMY TUBE
FDA Adverse Event
Death
·MOSS TUBES, INC.·Product code KNT·August 16, 2000
MOSS NASOJEJUNAL TUBE
FDA Adverse Event
MOSS TUBES, INC.·Product code FPD·May 4, 2007
MOSS
FDA Adverse Event
Death
·MOSS TUBES, INC.·Product code KNT·June 11, 1999
MOSS GASTROSTOMY TUBE (LOT #010202)
FDA Adverse Event
Other
·MOSS TUBES, INC.·Product code KNT·February 13, 2003
MOSS
FDA Adverse Event
Injury
·MOSS TUBES INC·Product code KNT·August 29, 1997
MOSS GASTROSTOMY TUBE
FDA Adverse Event
Malfunction
·MOSS TUBES, INC.·Product code KNT·August 27, 2020
MOSS PEG 18 146
FDA Adverse Event
Other
·MOSS TUBES, INC.·Product code FPD·January 27, 2011
MOSS G TUBE
FDA Adverse Event
Injury
·MOSS TUBES INC.·Product code KNT·March 21, 1997
MOSS GASTROSTOMY TUBE
FDA Adverse Event
Other
·MOSS TUBES, INC.·Product code KNT·October 20, 2004
MOSS GASTROSTOMY TUBE
FDA Adverse Event
Death
·MOSS TUBE INC.·Product code KNT·December 14, 2004