8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LEE BONE MARROW NEEDLES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
LEONE SPA
FDA UDI
LEONE SPA·08033707058182·DB TUBE MIM CONV 22 T-25 R+8 LR
LEONE SPA
FDA UDI
LEONE SPA·08033707064619·TUBE MIM CONV 22 T-25 R+8 LR
DECISIO HEALTH PATIENT DASHBOARD
FDA 510(k)
FDA Class 2
·Cardiovascular
AuST Steerable Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
INTERMATE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·May 31, 2014
ELEVATE ANTERIOR AND APICAL PROLAPSE REPAIR
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·November 13, 2012
HIGH FREQUENCY VENTED HUMIDIFICATION CHAMBER
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·August 24, 2010