4,201 results
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25ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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e.p.t. Digital Early Pregnancy Test
FDA UDI
Prestige Consumer Healthcare Inc.·00363736993030·e.p.t.® Digital 3 Ct
e.p.t. Direct
FDA UDI
Nfi Consumer Products·00045611963030·e.p.t. Direct 3 ct.
e.p.t. Direct
FDA UDI
Nfi Consumer Products·00045611962026·e.p.t. Direct 2 ct.
e.p.t. Analog
FDA UDI
Nfi Consumer Products·00045611952027·e.p.t. Analog 2 Ct
e.p.t. Early Pregnancy Test
FDA UDI
Prestige Consumer Healthcare Inc.·00363736952020·e.p.t.® Analog 2 Ct
e.p.t. Digital Early Pregnancy Test
FDA UDI
Prestige Consumer Healthcare Inc.·00363736992026·e.p.t.® Digital 2 Ct
e.p.t. Early Pregnancy test
FDA UDI
Prestige Consumer Healthcare Inc.·00363736953034·e.p.t.® Analog 3 Ct
N/A
FDA UDI
STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825008475·Diagnostic EP Catheter Cournand Curve, electrod...
N/A
FDA UDI
STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825007898·Steerable Diagnostic EP Catheter , STANDARD, 4 ...
EPT CERTAINTY PREGNANCY TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
EPT Menopause (FSH) Rapid Test
FDA UDI
Hangzhou AllTest Biotech Co., Ltd.·20045611954018·
ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)
FDA 510(k)
FDA Class 1
·Microbiology
NA
FDA UDI
GE Healthcare Finland Oy·00840682104128·
Cable, Return for RF/Bovie (EPT) (~10ft)
FDA UDI
Tz Medical, Inc.·00811331017434·Cable, Return for RF/Bovie (EPT) (~10ft)
EPT-1000 TC AUTOMATIC PERSONALITY MODULE (APM)
FDA Adverse Event
Malfunction
·EPT/A DIVISION OF BSC·Product code GXD·October 6, 2000
EPT-1000XP? RF ABLATION SYSTEM - FOOT SWITCH
FDA Adverse Event
Malfunction
·PLEXUS SERVICES CORPORATION·Product code OAD·June 20, 2013
BLAZER II HTD
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CARDIOVASCULAR DIVISION·Product code LPB·July 13, 2009
GENERATOR EPT-1000XP REFURBISHED
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC, EP TECHNOLOGIES·Product code LPB·June 27, 2008
RF CARDIAC ABLATION CONTROLLER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC, EP TECHNOLOGIES·Product code LPB·June 27, 2008
MAESTRO 3000 RF CARDIAC ABLATION POD REFURBIS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC, EP TECHNOLOGIES·Product code LPB·June 27, 2008