9 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Cryojet Plus (SHE-ACP001-1)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551082218·Elevator, sharp, curved, 4 mm, 18 cm
ELMED
FDA UDI
ELMED INCORPORATED·00842180148499·Hur Modified Mueller-type Femoral Neck Elevator...
Triathlon® Hinge Knee System; Triathlon® Revision Insert X3®
FDA 510(k)
FDA Class 2
·Orthopedic
SELECT 3D ARTERIAL CANNULA WITH CARMEDA BIOACTIVE SURFACE AND SELECT CAP ARTERIAL CANNULA WITH CARMEDA BIOACTIVE SURFACE
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2025
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·COVIDIEN·Product code OUT·November 6, 2014
PENUMBRA REPERFUSION CATHETER 041
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·July 18, 2013