41 results · 23ms · Sources: EU EUDAMED, US FDA

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INFINITY AMYLASE REAGENT (PROCEDURE NO. 580/568)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Preat

FDA UDI
Preat Corporation·00842092170823·Straumann® BL NC-compatible ASC Non-Engaging Ti...

Premier Universal Primer

FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·00348783000634·Premier Universal Primer Sample

Creation Willi Geller

FDA UDI
KLEMA Dentalprodukte GmbH·09010782022795·CC/ Approx. Dentine AD-2 orange

Creation Willi Geller

FDA UDI
KLEMA Dentalprodukte GmbH·ECWG0015691·CC/ Approx. Dentine AD-2 orange

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001569·artVeneer life upper anteriors, BOM, BL2

INTRABEAM® Flat Applicator Set 5.0 cm

FDA UDI
Carl Zeiss Meditec AG·04049539101532·

OPTIVU HDVD SYSTEM

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

MODEL 4000 EEG MONITOR WITH PSI (PSA4000)

FDA 510(k)
FDA Class 2 ·Neurology

E1 RINGLOC BIPOLAR 28X51MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 31, 2016

RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·June 15, 2017

E1 RINGLOC BIPOLAR 28X43MM

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code HBE·June 22, 2016

E1 HI-WALL LINER RINGLOC-X

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·June 2, 2017

RINGLOC BI-POLAR ACETABULAR COMPONENT

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·December 7, 2016

EON

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 30, 2014

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·March 11, 2013

VAMP SYSTEM WITH ARM-MOUNT RESERVOIR WITH PRESSURE TRANSDUCER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·February 25, 2011

E1 RINGLOC BIPOLAR 22X40MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 30, 2017

E1 RINGLOC BIPOLAR 28X54MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 26, 2016

E1 RINGLOC BIPOLAR 28X50MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 2, 2018