# KARDIUM Inc.

FEI: 3007603855
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Kardium Inc. (#10028366)

Address: 8518 Glenlyon Parkway, Unit 155, Burnaby British Columbia, V5J0B6, CA

Mandatory US Agent: Kardium US Inc.

## Products

Total registered: 1
Top product codes: QWA
Regulation §: 870.3955

Proprietary names: Globe® Catheter Cable Support, Globe® Platform

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007603855%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007603855