Reference Source

Acrostak (Schweiz) AG · 89-08 · SWITZERLAND

For Acrostak (Schweiz) AG · 89-08 · SWITZERLAND, import alert is 89-08; import alert name is "Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"; country is SWITZERLAND; product is Percutaneous Catheter; M CATH FLEXY; product code is 74 D - - QY Catheter, Percutaneous; date published is 05/09/2024; address is Stegackerstrasse 14 , Winterthur, Zurich SWITZERLAND, verified against its source on 2026-09-16.

Firm
Acrostak (Schweiz) AG verified
Import alert
89-08
Import alert name
"Detention Without Physical Examination of Devices without Approved PMA's or IDE's and Other Devices Not Substantially Equivalent or Without a 510(k)"
Country
SWITZERLAND verified
Address
Stegackerstrasse 14 , Winterthur, Zurich SWITZERLAND verified
Date published
05/09/2024 verified
Product code
74 D - - QY Catheter, Percutaneous verified
Product
Percutaneous Catheter; M CATH FLEXY verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

Acrostak (Schweiz) AG Date Published : 05/09/2024 Stegackerstrasse 14 , Winterthur, Zurich SWITZERLAND 74 D - - QY Catheter, Percutaneous Date Published: 05/09/2024 Desc: Percutaneous Catheter; M CATH FLEXY

accessdata.fda.gov, retrieved 2026-09-15

Source

Last verified against source: . Due for re-check by . This page as Markdown · OKF bundle · full dataset as JSON.

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