# BIODESIX, INC.

FEI: 3011854503
Status: Active
Establishment types: Manufacture Medical Device; Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Biodesix, Inc. (#10084036)

Address: 919 W Dillon Rd, Suite 100, Louisville, CO, US



## Products

Total registered: 1
Top product codes: PQD
Regulation §: 862.1675

Proprietary names: IQLung Specimen Collection Kit, Nodify Lung Specimen Collection Kit, Capillary Blood Specimen Collection Supplemental Pack

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223011854503%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3011854503