Acrostak Schweiz Ag

FDA Filings

This page includes the latest FDA filings for Acrostak Schweiz Ag. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3005086865
• FEI Number: 3005086865
• Name: Stephan Toupin
• Owner & Operator: Acrostak (Schweiz) AG
• Contact Address: Stegackerstrasse 14 ; WINTERTHUR CH-ZH Zurich 8409 CH
• Official Correspondent:
  • Ludwig Eckert
  • 41-52-2339554-x
• US Agent:
  • Stephan Toupin
  • Dawa Medical LLC
  • 786 7311159
  • 786 9998879
  • stoupin@dawamedical.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 350 south Miami Avenue, Suite 2403 ; Miami, FL 33130 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
GUDID 07640132622706 Acrostak (Schweiz) AG	M-CATH Flexy 820150732	2021-11-09
GUDID 07640132622690 Acrostak (Schweiz) AG	M-CATH Flexy 820135732	2021-11-09
GUDID 07640132622157 Acrostak (Schweiz) AG	M-CATH Microcatheter 750135730	2019-01-23
PMN K171176 | KRA Stephan Toupin [Acrostak (Schweiz) AG]	M-CATH Microcatheter	2018-03-09
PMN K171176 | DQY Stephan Toupin [Acrostak (Schweiz) AG]	M-CATH Microcatheter	2018-03-09
PMN K171176 Acrostak (Schweiz) AG	M-CATH Microcatheter	2017-09-15