7 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BONE GRAFT SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Dental
artegral HD
FDA UDI
Merz Dental GmbH·D7091973056·posteriors; shade B1; size S; upper jaw
TRYPTIC SOY AGAR (TSA) W/SXT - PRODUCT #P2933
FDA 510(k)
FDA Class 1
·Microbiology
DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9
FDA 510(k)
FDA Class 2
·Radiology
PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE
FDA Adverse Event
Malfunction
·MEDELA, INC.·Product code HGX·June 2, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·February 21, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 28, 2011