FDA.reportPublic FDA data

MEDIQUIP SDN. BHD.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96117123002807574MEDIQUIP SDN. BHD.1N2026-01-01Padang Lati Mukim Paya Batu 5 Jalan Santan Kangar Perlis MY 02450

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
17841167856607K990500KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946CEZL1999-09-28
17841481995592K881667KENDALL CURITY & KENGUARD RED RUBBER URETHRAL CATHGBM1988-08-12
17842030861464K860484CURITY & KENGUARD SILICONE COATED FOLEY CATHETERKOD1986-03-11
17841336206625K810630SILICONE ELASTOMER COATED LATEX FOLEYKOD1981-03-31
17841497118372K802875ARGYLE HEMATURIA BALLOON CATHETERKOD1980-12-16
17842025271280K041243DOVER RED RUBBER ROBINSON CATHETERKOD2004-07-07
17841909018218

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KOD42004-07-07
EZL11999-09-28
GBM11988-08-12