# STERIS Canada ULC

FEI: 3004097451
Status: Active
Establishment types: Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198
Owner/operator: STERIS Corporation (#10078069)

Address: 490 Boulevard Armand-Paris, QUEBEC, G1C 8A3, CA

Mandatory US Agent: STERIS Corporation

## Products

Total registered: 1
Top product codes: NZA
Regulation §: 876.1500

Proprietary names: Flow Unit 11 (QB-MF), Flow Unit 8 (QB-MF), Flow Unit 5 (QB-MF), Reliance DG Dry Germicide (5100) (MM-CFE), Flow Unit 2 (QB-MF), Flow Unit 1 (QB-MF), Flow Unit 10 (QB-MF), Flow Unit 7 (QB-MF), Flow Unit 6 (QB-MF), Flow Unit 3 (QB-MF)

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004097451%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004097451