Herpatech Ab

FDA Filings

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

FDA Registration(s)
Registration Number3012606445
FEI Number3012606445
NameCharlie Rector
Owner & OperatorHerpatech AB
Contact AddressVerkstadsgatan 4
?ngelholm SE-M Skane lan [SE-12] 26271 SE
Official Correspondent
  • Helena Berg
  • 46-72-2491043-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2900 37th Street NW, Building 003
Rochester, MN 55901 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Charlie Rector [Herpatech AB]
Universal Patch2019-02-18
Charlie Rector [Herpatech AB]
SP2003 BodyGuardian Mini Slide Strip2019-02-18
Charlie Rector [Herpatech AB]
SP2003 BodyGuardian Mini Easy Slide Strip2019-02-18
Charlie Rector [Herpatech AB]
BodyGuardian Mini Bridge SB20022016-03-29

Related Finance Registrations
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020091249275Anvers,Belgium -> New York/Newark Area, Newark, New JerseyUNIVERSAL PATCH HS CODE 30051000 MRN 20SEEBT3ZC38PNGH201 PKG
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