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

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Cleo

FDA 510(k)
FDA Class 2 ·Dental

RIGIDLOOP

FDA UDI
Medos International Sàrl·10886705022656·RIGIDLOOP Cortical Fixation Implant 20mm

OptoMonitor 3

FDA UDI
Opsens Inc·07540184320110·

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809665580399·Rod(CoCr), Ø5.5 x 110mm

GLOVETEX POWDER FREE WHITE NITRILE EXAMINATION GLOVES, NON-STERILE

FDA 510(k)
FDA Class 1 ·General Hospital

APOTECA DUG COMPOUNDING DOSING DEVICE,APOTECA I.V. TRANSFER SET

FDA 510(k)
FDA Class 2 ·General Hospital

Cable-Ready®

FDA UDI
Zimmer, Inc.·00889024039605·

Cable-Ready®

FDA UDI
Zimmer, Inc.·00889024039599·

LAP-BAND ACCESS PORT KIT (UNK SIZE)

FDA Adverse Event
Injury ·ALLERGAN·Product code LTI·July 13, 2011

ENDOPLEGE CORONARY SINUS CATHETER

FDA Adverse Event
Malfunction ·EDWARDS LIFESCIENCES·Product code DWF·July 2, 2011

ACRYSOF IQ TORIC

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·October 7, 2011

TREK CORONARY DILATATION CATHETER

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code LOX·November 6, 2014

ACCESS

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·September 1, 2011

ENERGEN

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 17, 2013

INTEGRIS ALLURA 15-12 (MONO)

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE·Product code IZI·March 9, 2011

INTERSTIM

FDA Adverse Event
Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 18, 2011

ALLURA XPER FD10

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE·Product code IZI·February 22, 2011

DRUG ELUTING PERMANET LEFT VENTRICULAR (LV) PACEMAKER ELECTRODE

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code OJX·August 12, 2023

DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code NVN·August 11, 2023

PALINDROME 19/36 KIT W/SLOT

FDA Adverse Event
Malfunction ·COVIDIEN·Product code MSD·September 23, 2011