Gambro Kathetertechnik Hechingen

FDA Filings

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

FDA Registration(s)
Registration Number3004367028
FEI Number3004367028
NameGAMBRO KATHETERTECHNIK HECHINGEN
Owner & OperatorGambro Renal Products, Inc.
Contact AddressOne Baxter Parkway
Deerfield IL 60015 US
Official Correspondent
  • Thomas P Sampogna
  • 1-224-9483016-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressLINSENAECKER 1
HECHINGEN Baden-Wurttemberg, DE-72379 DE
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
GAMBRO KATHETERTECHNIK HECHINGEN [Gambro Renal Products, Inc.]
Gamcath2015-10-27
GAMBRO KATHETERTECHNIK HECHINGEN [Gambro Renal Products, Inc.]
GAMCATH HIGH FLOW CATHETER2010-12-28

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