8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
VENTED NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668115145·EIPPERT SPATULA, DOUBLE-EDED
S TEST REAGENT CARTRIDGE BUN AND S TEST REAGENT CARTRIDGE CRE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CURAD SILVER ACTIVE GEL BANDAGE
FDA 510(k)
FDA Unclassified
·Unknown
TVT EXACT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·March 14, 2020
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL CO.·Product code MTA·January 24, 2013
COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 18, 2010
5MM PEEK MULTIFUNCTION HANDLE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code KOG·July 14, 2014