Curemed Nordic Ab

FDA Filings

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

FDA Registration(s)
Registration Number3015532181
FEI Number3015532181
NameCUREMED NORDIC AB
Owner & OperatorCureMed Nordic AB
Contact Addressgruvgatan 35B
Gothenburg SE-O Vastra Gotalands lan [SE-14] 42130 SE
Official Correspondent
  • Erik Puhasmagi
  • 46-031-475800-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Addressgruvgatan 35B
Gothenburg Vastra Gotalands lan [SE-14], 42130 SE
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
CUREMED NORDIC AB
Replacement Clamp2019-06-21

Related Finance Registrations

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