# Vitrolife GmbH

FEI: 3003843927
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Vitrolife GmbH (#9087379)

Address: Roedersteinstrasse 6, Landshut Bavaria, 84034, DE

Mandatory US Agent: Vitrolife Inc.

## Products

Total registered: 1
Top product codes: MRX
Regulation §: 884.6200

Proprietary names: Octax LaserShotM, Octax NaviLase

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223003843927%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3003843927