FDA.reportPublic FDA data

MEDIPLUS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30059563113005956311MEDIPLUS (INDIA) LIMITED1N2026-01-011261-1262, M.I.E. Part B, Bahadurgarh-124507 Haryana (India) Bahadurgarh Haryana IN 124507
30113081393011308139MEDIPLUS MANUFACTURING LTD.1N2020-04-25Unit 8 The Gateway Centre, Cressex Business Park Coronation Road Coronation Road Buckinghamshire GB HP12 3SU

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
05055140702807Mediplus - Capnomask™ Adult Oxygen mask+4401494551200help@mediplusuk.com
05055140703170MMS - Double lumen catheter, 8fr, latex free+4401494551200help@mediplus.co.uk
05055140703187MMS - Double lumen catheter, 6fr, latex free+4401494551200help@mediplus.co.uk
05055140703392TIMM - Gas tubing kit+4401494551200help@mediplus.co.uk
05055140703415TIMM - Water pump tubing kit+4401494551200help@mediplus.co.uk
05055140703866Prometheus - Pathway Anorectal response catheter, 14Fr+4401494551200help@mediplus.co.uk
15055140702804Mediplus - Capnomask™ Adult Oxygen mask+4401494551200help@mediplusuk.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3069671214445106K210037Pluski Safe 1 Safety IV CatheterFOZ2022-03-25
1760821350740357K132890SUPRAPUBIC CATHETER AND INTRODUCER SETKOB2014-01-17
1760821198021716
1760821532099478

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FOZ12022-03-25
KOB12014-01-17

PMN#

GUDID#

80 records. Showing 1-40. Next