# STERILMED, INC.

FEI: 3011276773
Status: Active
Establishment types: Reprocess Single-Use Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: STERILMED, INC. (#9030419)

Address: 5010 Cheshire Pkwy N Ste 2, Plymouth, MN, US



## Products

Total registered: 1
Top product codes: OWQ
Regulation §: 870.1200

Proprietary names: Reprocessed Ultrasound Catheter

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223011276773%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3011276773