7 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Selectra Lead Implantation System
FDA 510(k)
FDA Class 2
·Cardiovascular
HEALIX ADVANCE PEEK 3 SUTURE ANCHOR w/DYNACORD
FDA UDI
Medos International Sàrl·10886705029549·HEALIX ADVANCE PEEK 3 SUTURE ANCHOR w/DYNACORD ...
XLTEK SLEEP SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
ANATOMIC PEEK CERVICAL FUSION SYSTEM CORNERSTONE PSR CERVICAL FUSION SYSTEM PEEK PREVAIL CERVICAL INTERBODY DEVICE CAPST
FDA 510(k)
FDA Class 2
·Orthopedic
PUMP MMT-715NAS PRDGM INS V2.1 SK EN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·November 3, 2008
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 24, 2011
CLINITRON RITEHITE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code INX·July 3, 2013