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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HEMOCATH REPAIR KIT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780399322·Integra® Jarit® Obwegeser Ramus Retractor, 9-1/...
UniTip Catheter
FDA UDI
Unisensor AG·07640172971819·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971796·
UniTip Catheter
FDA UDI
Unisensor AG·07640172971802·
LASER ENDOSCOPIC DECOMPRESSION KIT, MODEL 1100, AND PERCUTANEOUS DISCECTOMY KIT, MODEL 1120
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RESPIRONICS REUSABLE HEATED TUBING
FDA 510(k)
FDA Class 2
·Anesthesiology
INTERSTIM
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code EZW·May 30, 2014
INTERSTIM II
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 20, 2012
EPIC II CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER CORP. MEDICAL DIV.·Product code FNL·September 10, 2010