Medisize Ireland L T D

FDA Filings

This page includes the latest FDA filings for Medisize Ireland 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 Number8020864
FEI Number3005737257
NameMEDISIZE IRELAND LTD.
Owner & OperatorPhillips-Medisize, LLC
Contact Address1201 Hanley Road
Hudson WI 54016 US
Official Correspondent
  • Lisa Short
  • x-715-5771236-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressHIGH ROAD
LETTERKENNY Donegal, -- IE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
MEDISIZE IRELAND LTD. [Phillips-Medisize, LLC]
Fluent Inflation Device2017-12-18
MEDISIZE IRELAND LTD. [Phillips-Medisize, LLC]
TECA Myoject - Luer lock - Disposable needle electrode,Bo-ject? DHN Disposable Hypodermic Needle Electrode2017-12-18
MEDISIZE IRELAND LTD. [Phillips-Medisize, LLC]
CT ExpresTM 3D Contrast Media Delivery System2017-12-18
MEDISIZE IRELAND LTD. [Phillips-Medisize, LLC]
VSI Torque Device2015-12-11
MEDISIZE IRELAND LTD. [Phillips-Medisize, LLC]
TECA Myoject - Luer lock - Disposable needle electrode2014-11-13
MEDISIZE IRELAND LTD. [Phillips-Medisize, LLC]
Injection needle (37mm x 27G) Disposable Hypodermic Needle Electrode2014-11-13

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