4,201 results · 25ms · Sources: EU EUDAMED, 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