15 results · 20ms · Sources: EU EUDAMED, US FDA

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COMBIPORT FLUID LAVAGE DEVICE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Sklar

FDA UDI
SKLAR CORPORATION·10649111057120·LITTAUER CUT FCP STL 5 INCHES

TRANSEND EX 14 GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009

HYDENT

FDA 510(k)
FDA Class 1 ·Dental

ALBUMIN TEST, HMA ALBUMIN TEST

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

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FDA Adverse Event
Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

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FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

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FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

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FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

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FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

VASOVIEW HEMOPRO 2

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR LLC·Product code GEI·June 30, 2014

SCREW LOCKING

FDA Adverse Event
Injury ·SYNTHES USA·Product code KWP·February 21, 2013

IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 26, 2011

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FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010

L.C. 5000/CE 2-CHANNEL PUMP (50/CASE)

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·August 22, 2013