# Seisa Europe s.r.o.

FEI: 3006891655
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Seisa Europe s.r.o. (#10024045)

Address: priemyselna 4, myjava Trenciansky, 90701, SK

Mandatory US Agent: Tekni-Plex Healthcare

## Products

Total registered: 1
Top product codes: FGE
Regulation §: 876.5010

Proprietary names: Zimmon biliary stent

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223006891655%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3006891655