Meddev Manufacturing Sdn Bhd

FDA Filings

This page includes the latest FDA filings for Meddev Manufacturing Sdn Bhd. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3006307105
FEI Number3006307105
NameMedDev Manufacturing Sdn Bhd
Owner & OperatorSeeBreath AB
Contact AddressBirger Jarlsgatan 2
Stockholm SE-AB Stockholms lan [SE-01] 11434 SE
Official Correspondent
  • Anette Sjogren
  • 46-46-295358-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressNo 115 Jalan Serunai, 1, Kawasan 3
Klang Selangor, 41200 MY
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
MedDev Manufacturing Sdn Bhd [SeeBreath AB]
CapnoDura Combi, CapnoDura Pedi2012-08-10

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020090914072Singapore,Singapore -> Norfolk, VirginiaDETECTOR13 PKG
202008221323Xiamen,China (Mainland) -> Norfolk, VirginiaDETECTOR16 PKG
2020082117010Singapore,Singapore -> Tacoma, WashingtonDETECTOR12 PKG
202008181076Xiamen,China (Mainland) -> Norfolk, VirginiaDETECTOR20 PKG
2020062210118Singapore,Singapore -> Norfolk, VirginiaDETECTOR13 PKG
2020052514446Port Swettenham,Malaysia -> Savannah, GeorgiaDETECTOR LARGE17 PKG
202005076389Singapore,Singapore -> Los Angeles, CaliforniaDETECTOR LARGE1 PKG
202004308954Singapore,Singapore -> Norfolk, VirginiaDETECTOR LARGE11 PKG
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