10 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS
FDA 510(k)
FDA Class 2
·General Hospital
Irrigation/Aspiration set for TURP (Urology) - 2 spikes - pump segment
FDA UDI
Promepla·03700512901839·
Ultracheck
FDA UDI
Statcorp Medical·10841522100932·BP CUFF,MIDMARK, REUSABLE, 1T, INFANT, HP,EA
COPPERHEAD CERVICAL INTERBODY CAGE
FDA Adverse Event
Injury
·EMINENT SPINE·Product code ODP·January 8, 2016
RUSCH POLYFLEX STENT FOR THE ESOPHAGUS WITH INTRODUCER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
COMPUMEDICS E-SERIES EEG SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
LNOP MP12 PATIENT CABLE
FDA Adverse Event
Malfunction
·MASIMO CORPORATION·Product code DQA·May 15, 2015
UNIFY ASSURA CRT-D
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·May 2, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 15, 2014
PRODISC-L SUPERIOR ENDPLATE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code MJO·May 6, 2011