372 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APC PLUS ADHESIVE
FDA 510(k)
FDA Class 2
·Dental
APC PLUS, CLARITY, MINI UNI-TWIN, VICTORY SERIES
FDA Adverse Event
Injury
·3M UNITEK·Product code DYH·May 9, 2012
Safco lead-free x-ray aprons
FDA UDI
SAFCO DENTAL SUPPLY CO.·D7231020394·Lead-free thyroid protector beige
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040051310·FILE - Channels PT Platinum - C4 21MM
Midway Select
FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717103896·Stainless Steel K Files (Hand), Size # 08, Leng...
BARD PERIPHERAL VASCULAR, INC.
FDA registration
BARD PERIPHERAL VASCULAR, INC.·49 products·🇺🇸 United States
JMS APHERESIS NEEDLE SET ACCORDION TYPE
FDA 510(k)
FDA Class 2
·General Hospital
CRAFT DUO-VAC SUCTION UNIT AND CRAFT SUCTION UNIT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
G2 FILTER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 25, 2019
G2 VENA CAVA FILTER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·April 16, 2019
G2 FILTER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·April 16, 2019
G2 FILTER
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·July 25, 2019
2020394-2007-00203
FDA Adverse Event
Malfunction
·Product code LIT·June 22, 2007
2020394-2007-00310
FDA Adverse Event
Malfunction
·Product code DTK·November 26, 2007
2020394-1997-00005
FDA Adverse Event
Injury
·Product code DSY·July 25, 1997
2020394-1997-00002
FDA Adverse Event
Injury
·Product code MCI·May 1, 1997
2020394-2006-00007
FDA Adverse Event
Injury
·Product code DTK·January 6, 2006
2020394-2006-00348
FDA Adverse Event
October 31, 2006
2020394-1999-00018
FDA Adverse Event
Injury
·December 30, 1999
2020394-1999-00010
FDA Adverse Event
Injury
·November 24, 1999