Guenter Stoffel Medizintechnik G M B H

FDA Filings

This page includes the latest FDA filings for Guenter Stoffel Medizintechnik G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number8010370
FEI Number4417
NameFranz Menean
Owner & OperatorGUENTER STOFFEL MEDIZINTECHNIK GMBH
Contact AddressKANTSTR. 37 --
WURMLINGEN DE-BW Baden-Wurttemberg D-78573 DE
Official Correspondent
  • DIETER - STOFFEL
  • 49-7461-5890-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address112 CORPORATE DR
Portsmouth, NH 03801 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Franz Menean [GUENTER STOFFEL MEDIZINTECHNIK GMBH]
Anastomosis Blade Holder2009-07-29
Franz Menean [GUENTER STOFFEL MEDIZINTECHNIK GMBH]
Disposable Bioptome2007-12-01
Franz Menean [GUENTER STOFFEL MEDIZINTECHNIK GMBH]
INSTO BIOPSY FORCEPS2004-11-10
Franz Menean [GUENTER STOFFEL MEDIZINTECHNIK GMBH]
INSTO NEEDLE HOLDER2004-11-10
Franz Menean [GUENTER STOFFEL MEDIZINTECHNIK GMBH]
INSTO MICRO INSTRUMENTS2001-09-05

Related Finance Registrations
NCAGE CodeCF051GUENTER STOFFEL MEDIZINTECHNIK GMBH
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.