# VITROLIFE SWEDEN AB

FEI: 3003995932
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: VITROLIFE AB (#9037178)

Address: Gustaf Werners Gata 2, Vastra Frolunda Vastra Gotaland, SE-421 32, SE

Mandatory US Agent: Vitrolife Inc.

## Products

Total registered: 1
Top product codes: HIO
Regulation §: 884.1550

Proprietary names: Amniocentesis Needle

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003995932%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003995932