Gp Lumut

FDA Filings

This page includes the latest FDA filings for Gp Lumut. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011189071
FEI Number3011189071
NameMichael van der Woude
Owner & OperatorGP Lumut
Contact AddressLot No. 15652, Kawasan Perindustrian Kampung Acheh
Sitiawan MY-08 Perak 32000 MY
Official Correspondent
  • Punitha P Samy
  • 60-5679-2288-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2500 Bee Cave Road Building 1, Suite 300
Austin, TX 78746 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Develop Specifications But Do Not Manufacture At This Facility




Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.