Guenter Bissinger Medizintechnik G M B H

FDA Filings

This page includes the latest FDA filings for Guenter Bissinger 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 Number8010456
FEI Number3002477156
NameFranz Menean
Owner & OperatorGUENTER BISSINGER MEDIZINTECHNIK GMBH
Contact AddressHans-Theisen-Str. 1
TENINGEN DE-BW Baden-Wurttemberg D-79331 DE
Official Correspondent
  • MATTHIAS - BISSINGER
  • 049-7641-91433-0
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address112 CORPORATE DR
Portsmouth, NH 03801 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
Guenter Bissinger Medizintechnik GmbH
Supra Non-Stick Bipolar Forceps2022-11-17
GUENTER BISSINGER MEDIZINTECHNIK GMBH
Bissinger Monopolar Cables2015-02-20
GUENTER BISSINGER MEDIZINTECHNIK GMBH
CLARIS NON-STICK BIPOLAR FORCEPS2005-07-29
GUENTER BISSINGER MEDIZINTECHNIK GMBH
BITECH BIPOLAR SCISSORS2004-10-27
GUENTER BISSINGER MEDIZINTECHNIK GMBH
BISSINGER CABLES, CAT. NO. 801000XX1998-08-06
GUENTER BISSINGER MEDIZINTECHNIK GMBH
BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS1998-05-21

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