Mediplus Manufacturing L T D

FDA Filings

This page includes the latest FDA filings for Mediplus Manufacturing L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011308139
FEI Number3011308139
NameMEDIPLUS MANUFACTURING LTD.
Owner & OperatorMEDIPLUS MANUFACTURING Ltd.
Contact AddressUnit 8 The Gateway Centre Cressex Business Park
High Wycombe GB-BKM Buckinghamshire HP12 3SU GB
Official Correspondent
  • EMMA GRAY
  • 44-1494-551200-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressUnit 8 The Gateway Centre, Cressex Business Park Coronation Road
Coronation Road Buckinghamshire, HP12 3SU GB
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
MEDIPLUS MANUFACTURING LTD.
CATHETER, SUPRAPUBIC (AND ACCESSORIES)2014-11-02
MEDIPLUS MANUFACTURING LTD.
CATHETER, CYSTOMETRIC, HYDRAULIC2014-11-02
MEDIPLUS MANUFACTURING LTD.
ACCESSORIES, CATHETER2014-11-02
MEDIPLUS MANUFACTURING LTD.
ACCESSORIES, CATHETER2014-11-02
MEDIPLUS MANUFACTURING LTD.
DEVICE, CYSTOMETRIC, HYDRAULIC2014-11-02

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