81 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HBA1C LINEARITY SET
FDA 510(k)
FDA Class 1
·Clinical Chemistry
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809763503115·Cannulated Long-Arm Multi-Axial Screw Driver
LATERAL DISTAL FIBULA PLATE, XS, 10-HOLE, RIGHT
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665029925·
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193103365·HA PEEK EVOS Curved, , 10mmx10mmx 26mm , FLAT 0...
CONMED
FDA UDI
Conmed Corporation·10845854018903·UNIVERSAL HOSE, 10'
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809841732·FOR MEN 15-20 MM HG KNEE HIGH CLOSED TOE LARGE ...
STC METHADONE INTERCEPT MICRO-PLATE EIA, MODEL 11421
FDA 510(k)
FDA Class 2
·Clinical Toxicology
MODIFICATION TO LR 5200 FILM RECORDER
FDA 510(k)
FDA Class 2
·Radiology
UNIVERSAL HOSE
FDA Adverse Event
Malfunction
·LINVATEC·Product code HSZ·March 3, 2003
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·October 31, 2025
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 19, 2026
ASR UNI FEMORAL IMPL SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·April 11, 2013
KENTROX A+ 75/15 STEROID
FDA Adverse Event
Malfunction
·BIOTRONIK, GMBH AND CO.·Product code LWS·May 21, 2008
EASYTRAK 2
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·April 12, 2011
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 1, 2026
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·May 14, 2026
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 9, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·December 22, 2025
ARCHITECT CA19-9XR
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·April 3, 2026
ALINITY I CA 19-9XR REAGENT KIT
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code NIG·November 4, 2025