# Siemens Healthineers AG

FEI: 3000275399
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Siemens Healthineers AG (#8010024)

Address: RONTGENSTRASSE 2, RUDOLSTADT Thuringia, 07407, DE

Mandatory US Agent: SIEMENS MEDICAL SOLUTIONS USA, INC.

## Products

Total registered: 1
Top product codes: ITY
Regulation §: 892.1760

Proprietary names: CHRONON Family, Optitop Family, Megalix Family, TR Family, DURA Family, Vectron Family, STRATON Family, Athlon Family, Optilix Family, SIREPHOS Family

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223000275399%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3000275399