FDA Device Establishments · JSON-LD · Markdown

Seisa Europe s.r.o.

FEI 3006891655 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3006891655
Owner / OperatorSeisa Europe s.r.o. (#10024045)
Addresspriemyselna 4, myjava Trenciansky, 90701, SK
Mandatory US AgentTekni-Plex Healthcare
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)FGE
Regulation § (21 CFR)876.5010
Proprietary namesZimmon biliary stent

External sources

Source: openFDA. Public-domain (CC0).