# ANRIWELL

FEI: 3043513123
Status: Active
Establishment types: Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Anriwell (#10095154)

Address: 2062 Business Center Dr Ste 125, Irvine, CA, US



## Products

Total registered: 1
Top product codes: DXN
Regulation §: 870.1130

Proprietary names: AW-301, Anriwell Pressia

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223043513123%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3043513123