8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HICKMAN PLASTIC SUBCUTANEOUS PORT
FDA 510(k)
FDA Class 2
·General Hospital
Legacy™4 Implant
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307102816·Ø3.2 x 13 Platform 3.0mmD
O.I.C. TITANIUM
FDA UDI
Stryker Corporation·07613327261943·DISTRACTOR
SHARIA-LH RIA KIT FOR QUANTITATION HORMO
FDA 510(k)
FDA Class 1
·Clinical Chemistry
THERABOND ANTIMICROBIAL BARRIER SYSTEMS
FDA 510(k)
FDA Unclassified
·Unknown
MINICAP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 13, 2014
FLO-GARD 6201 VOLUMETRIC INFUSION PUMP 2M8063,
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 18, 2010
FREESTYLE LITE
FDA Adverse Event
Injury
·Product code NBW·December 13, 2012