108 results · 25ms · Sources: EU EUDAMED, US FDA

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VENOUS M/A INTERNAL JUGULAR KIT

FDA 510(k)
FDA Class 2 ·Cardiovascular

Polishers

FDA UDI
DFS - DIAMON GmbH·04057176152237·2ceram polisher cup RA

Bioseal Inc.

FDA UDI
BIOSEAL·00630094180069·Hemorrhoid Bands

ACUMED

FDA UDI
Acumed LLC·10806378043505·T15 Hexalobe Driver

Arthrex®

FDA UDI
ARTHREX, INC.·00888867042469·2 HOLE DBL COMP PLATE, 20MM

NANCY NAIL AND ENDCAP KIT

FDA UDI
Biomet Orthopedics, LLC·00887868032851·

iNSitu™ Hip System

FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127026836·Shortened Dual Taper Broach, Size 20

MODIFICATION TO 3M TEGADERM CHG DRESSING

FDA 510(k)
FDA Unclassified ·Unknown

PBN FALLOPIAN TUBE CATHETER SYSTEM

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE·Product code IOR·May 8, 2014

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 22, 2012

INRATIO

FDA Adverse Event
Malfunction ·BIOSITE INCORPORATED·Product code GJS·August 4, 2010

NFix II System 150 mm, Catalog number NX60150-1 spinal fusion surgery

FDA Recall
Terminated ·Synthes Spine·Product code NQP·November 7, 2008

NFix II System 200 mm, Catalog number NX60200-1. spinal fusion surgery

FDA Recall
Terminated ·Synthes Spine·Product code NQP·November 7, 2008

N-Hance System 150 mm, Catalog number NH60150-1. spinal fusion surgery

FDA Recall
Terminated ·Synthes Spine·Product code NQP·November 7, 2008

NFlex Stabilization System 150 mm, Catalog number NF60150-1. spinal fusion surgery

FDA Recall
Terminated ·Synthes Spine·Product code NPQ·November 7, 2008

NFlex Stabilization System 200 mm, Catalog number NF60020-1. spinal fusion surgery

FDA Recall
Terminated ·Synthes Spine·Product code NPQ·November 7, 2008

TI N-Hance Rod 150 mm Sterile, Catalog number 04.600.715.02S spinal fusion surgery

FDA Recall
Terminated ·Synthes Spine·Product code NQP·November 7, 2008

Synthes Bone Marrow Aspiration System, Sterile, 11 gauge, 15cm needle (without side holes) Indicated for aspirating bone marrow

FDA Recall
Terminated ·Synthes USA (HQ), Inc.·Product code FMF·January 26, 2011

Synthes Medullary Tubes

FDA Recall
Terminated ·Synthes USA (HQ), Inc.·Product code LXH·April 1, 2010