9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LO-PROFILE EXTENSION SET
FDA 510(k)
FDA Class 2
·General Hospital
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665582461·MIS Cannulated Screw, Ø5.5 x 60mm, Ø5.5mm Rod
NOVA 12 ANALYZER
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ZEPHYR INFUSION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
OMNIPOD DASH¿ INSULIN MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·June 3, 2020
INQUIRY STEERABLE CATHETER 6F, 1110-6-5-L
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL, IRVINE·Product code DRF·November 5, 2010
UNKNOWN REJUVENATE HIP STEM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·January 10, 2013
END MODULAR HUM STEM D12 HA
FDA Adverse Event
Injury
·DEPUY FRANCE S.A.S.-SAINT PRIEST 3003895575·Product code HSD·July 7, 2014
BMT 360 TIBIAL TRAY 79MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 26, 2020