Scanfil Atvidaberg Ab

FDA Filings

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

FDA Registration(s)
Registration Number3008727520
FEI Number3008727520
NameSCANFIL ATVIDABERG AB
Owner & OperatorScanfil Atvidaberg AB
Contact AddressOrsatter
Atvidaberg SE-E Ostergotlands lan [SE-05] 59780 SE
Official Correspondent
  • Karin Skullman
  • 046-72-9660488-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressOrsatter
Atvidaberg Ostergotlands lan [SE-05], 59780 SE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
SCANFIL ATVIDABERG AB
IQoolTM Warm System2019-04-01
SCANFIL ATVIDABERG AB
Lucas 32018-02-14
SCANFIL ATVIDABERG AB
Lucas 32016-11-25
SCANFIL ATVIDABERG AB
Lucas 22010-12-07
SCANFIL ATVIDABERG AB
Lucas2010-12-07

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020090325444Norrkoping,Sweden -> Charleston, South CarolinaMICROWAVE HS-CODE 9027200015 PKG
2020090225079Norrkoping,Sweden -> Charleston, South CarolinaMICROWAVE HS-CODE 9027200015 PKG
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