FDA Device Establishments · JSON-LD · Markdown

Vitrolife GmbH

FEI 3003843927 · Manufacture Medical Device · Status: Active

FEI Number3003843927
Owner / OperatorVitrolife GmbH (#9087379)
AddressRoedersteinstrasse 6, Landshut Bavaria, 84034, DE
Mandatory US AgentVitrolife Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)MRX
Regulation § (21 CFR)884.6200
Proprietary namesOctax LaserShotM; Octax NaviLase

External sources

Source: openFDA. Public-domain (CC0).