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NIPRO CANADA CORPORATION

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
80203473005612924NIPRO CANADA CORPORATION1N2026-01-01199 ST. DAVID STREET LINDSAY Ontario CA K9V 5K7

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
95501432859851K963748BIO-PLEXUS DROP-IT NEEDLE HOLDERFMI1997-06-06
95501343522491K850009EVANS, VAS-CATH EPIDURAL NEEDLE & CATHETERBSO1985-05-13
95501012974522K833112TUBING FOR CARDIOPULMONARY BYPASSDWF1983-11-28
95501810651847K080174PHLEBOTOMY BAG WITH VALVE & 17G X 1, MODEL CM-PH17X1B, CM-PH17X1CLHI2008-04-23
95501755157727K04267214F DUAL FLOATING DIALYSIS CATHETER/TRAYMSD2005-03-23
95501456211774
95502067657039
95501307560346
95501424920566
95502013830685

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LHI12008-04-23
MSD12005-03-23
FMI11997-06-06
BSO11985-05-13
DWF11983-11-28