592 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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