Wedeka Industrie Ter Apel

FDA Filings

This page includes the latest FDA filings for Wedeka Industrie Ter Apel. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3015220768
FEI Number3015220768
NameWEDEKA Industrie Ter Apel
Owner & OperatorWedeka Industrie Veendam
Contact AddressPhoenixweg 2
Veendam NL-GR Groningen 9641 KS NL
Official Correspondent
  • T. Katerberg
  • 31-598-614152-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressNomdenweg 1
Ter Apel, 9561 AM NL
Establishment TypeRepack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
WEDEKA Industrie Ter Apel [Wedeka Industrie Veendam]
Wartie Advanced Reover/Compound W2019-01-08
WEDEKA Industrie Ter Apel [Wedeka Industrie Veendam]
Wartie Wart remover/Compound W2019-01-08

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