Medi Plus Instrumente G M B H

FDA Filings

This page includes the latest FDA filings for Medi Plus Instrumente 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 Number: 8010935
• FEI Number: 3002807646
• Name: Beate Weiss-Krull
• Owner & Operator: medi-plus Instrumente GmbH
• Contact Address: Sattlerstrasse 11 ; Tuttlingen DE-BW Baden-Wurttemberg 78532 DE
• Official Correspondent:
  • Bruno Mattes
  • 049-7461-12825-x
• US Agent:
  • Beate Weiss-Krull
  • Beate Weiss-Krull, Attorney at Law
  • 503 2340355
  • bea@weisskrull-law.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 1050 SW 6th Ave., Suite 1100 ; Portland, OR 97204 US
• Establishment Type:
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device