7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MODIFIED PK300 AUTOMATIC EIA ANALYZER
FDA 510(k)
FDA Class 1
·Clinical Chemistry
C. PTH RADIOIMMUNOASSAY KIT-CPTHK
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CLIRANS TE08 HOLLOW FIBER DIALYZER
FDA 510(k)
FDA Class 2
·Ophthalmic
RECAP SHELL COCR PC 48/42MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·June 25, 2014
5.0MM TI ANGULAR STABLE LCKNG SCR T25 48MM F/IM NAILS-STER
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HSB·January 2, 2013
STRETCHER
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIVISION·Product code FPO·November 2, 2010
Azurion 7 M20 FlexArm system (Software version R2.x) with Maquet Magnus Table (Software version 05.02.12)
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 7, 2024