FDA.report

UNISENSOR AG

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
97106393003126165UNISENSOR AG1N2020-04-25BAHNSTRASSE 12A ATTIKON Zurich CH CH-8544

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
193651823947258K102801PHTIP DISPOSABLE ISFET CATHETERFFX2010-10-26
193651384006872K062222UNITIP HIGH RESOLUTION CATHETERFFX2007-03-15
193651848764620K022023COMPASS ESOPHAGEAL PRESSURE CATHETER, MODEL GIE-8500, COMPASS ANO-RECTAL PRESSURE CATHETER, MODEL GIA-8500KLA2003-01-07
193651364561352K003580UNITIP GASTROINTESTINAL PRESSURE SENSOR CATHETERFFX2001-07-31
193651192928011
193651500764625
193651800696074

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
FFX32010-10-26
KLA12003-01-07

PMN

GUDID

200 records. Showing 1-40. Next