FDA.reportPublic FDA data

QLRAD

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30069487453006948745QLRAD1N2026-01-01Damsluisweg 6 Almere Flevoland NL 1332 EC
30104722813010472281Qlrad Inc1Y2026-01-0180 SW 8th street, suite 2000 Miami FL US 33130

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
08719326258201QLRAD - RectalPro75 with 100 cc Syringe+13054378550awinkel@qlrad.com
08719326258218QLRAD - RectalPro75+13054378550awinkel@qlrad.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
854951846327351K180478RectalPro 75 Endorectal BalloonPCT2018-11-13
854951954163986K112057KDL SYRINGES AND NEEDLEFMF2011-12-14
1623301393179736

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PCT12018-11-13
FMF12011-12-14

PMN#

GUDID#