8 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AQ HYDROPHILIC STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UNIVERSA FIRM URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·March 26, 2018
P.F.C. SIGMA
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295238607·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...
S1 ORAL PACKING
FDA 510(k)
FDA Unclassified
·Unknown
Biopor Porous Polyethylene Implants
FDA 510(k)
FDA Class 2
·Neurology
HOLDING SLEEVE - LONG
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code LXH·February 11, 2013
SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA
FDA Adverse Event
Malfunction
·STAAR SURGICAL CO.·Product code HQL·January 7, 2011
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 28, 2014