21 results · 24ms · Sources: EU EUDAMED, US FDA

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First Sign Drug of Abuse Dip Card Test (MDMA, EDDP, Nortriptyline), First Sign Drug of Abuse Cup Test (MDMA, EDDP, Nortriptyline)

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

Oxford Partial Knee System

FDA UDI
Biomet Uk Ltd·05019279073047·Anatomic Meniscal Bearing Right Medial

ELEMENT BLOOD GLUCOSE TEST SYSTEM

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

UROSTATION 3D PROSTATE SUITE

FDA 510(k)
FDA Class 2 ·Radiology

FORTIFY DR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL INC. CRMD·Product code LWS·January 13, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

RETAIN-SLEEVE LONG F/MATRIX 5.5

FDA Adverse Event
Malfunction ·SYNTHES MONUMENT·Product code LXH·June 11, 2013

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·December 23, 2016

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·March 23, 2017

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·October 24, 2016

RHYTHMIA HDX

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·February 20, 2019

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Malfunction ·COOK INC·Product code MMX·October 29, 2018

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·August 3, 2018

SET SCREWDRIVER, FLEXIBLE SHAFT GAMMA3® 4 MM

FDA Adverse Event
Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·January 2, 2019

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·September 7, 2016

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·April 30, 2018

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·April 14, 2017

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·June 14, 2018

INDY OTW VASCULAR RETRIEVER

FDA Adverse Event
Injury ·COOK INC·Product code MMX·April 20, 2017