FDA Device Establishments · JSON-LD · Markdown

SUNRISE SA

FEI 3022505448 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3022505448
Owner / OperatorSUNRISE (#10084974)
AddressChaussee de marche 598 boite 2, NAMUR, 5101, BE
Mandatory US AgentQserve Group US, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)QRS
Regulation § (21 CFR)868.2376
Proprietary namesSUNRISE DEVICE

External sources

Source: openFDA. Public-domain (CC0).