Poeppelmann G M B H Co Kg Kunststoffwerk Werkzeugbau

FDA Filings

This page includes the latest FDA filings for Poeppelmann G M B H Co Kg Kunststoffwerk Werkzeugbau. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3000261882
FEI Number3000261882
NamePOEPPELMANN GMBH CO KG KUNSTSTOFFWERK WERKZEUGBAU
Owner & OperatorPOEPPELMANN GMBH CO KG KUNSTSTOFFWERK WERKZEUGBAU
Contact AddressBakumer Strasse 73
Lohne DE-NI Niedersachsen 49393 DE
Official Correspondent
  • Martin Hammoor
  • 049-4442-982-8040
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressBakumer Strasse 73
Lohne Niedersachsen, 49393 DE
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
POEPPELMANN GMBH CO KG KUNSTSTOFFWERK WERKZEUGBAU
BabyFlow Neo Mask2014-08-05

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