FDA Device Establishments · JSON-LD · Markdown
FEI 3007603855 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3007603855 |
|---|---|
| Owner / Operator | Kardium Inc. (#10028366) |
| Address | 8518 Glenlyon Parkway, Unit 155, Burnaby British Columbia, V5J0B6, CA |
| Mandatory US Agent | Kardium US Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QWA |
| Regulation § (21 CFR) | 870.3955 |
| Proprietary names | Globe® Catheter Cable Support; Globe® Platform |
Source: openFDA. Public-domain (CC0).