Hans Karl Seid

FDA Filings

This page includes the latest FDA filings for Hans Karl Seid. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 8010523
• FEI Number: 3006720810
• Name: Franz Menean
• Owner & Operator: HANS KARL SEID
• Contact Address: Zeppelinstr. 10 --; DENKINGEN DE-BW Baden-Wurttemberg 78588 DE
• Official Correspondent:
  • Hans K Seid
  • 049-7424-1316-x
• US Agent:
  • Franz Menean
  • MEDAGENT, Inc.
  • 603 5702039
  • 603 5702055
  • mail@medagent-usa.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 112 CORPORATE DR ; Portsmouth, NH 03801 US
• Establishment Type: Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
FXE Franz Menean [HANS KARL SEID]	Trans Speculum	2012-11-08
FXE Franz Menean [HANS KARL SEID]	Speculum	2012-11-08
EPY Franz Menean [HANS KARL SEID]	ENT SPECULUM	1986-06-05