FDA Device Establishments · JSON-LD · Markdown
FEI 1000589001 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 1000589001 |
|---|---|
| Owner / Operator | ARJOHUNTLEIGH AB (#8010077) |
| Address | DIAGNOSTIC PRODUCT DIVISION, 35 PORTMANMOOR ROAD, CARDIFF, SOUTH GLAMORGAN, CF24 5HN, GB |
| Mandatory US Agent | Arjo, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | JOW |
| Regulation § (21 CFR) | 870.5800 |
| Proprietary names | Hydroven 12 Garments (HUNTLEIGH HEALTHCARE - SPEC. DEVELOPER & COMPLAINTS, POZNAN - CONTRACT MFR); Hydroven 12 Pump (HUNTLEIGH HEALTHCARE - SPEC. DEVELOPER & COMPLAINTS,SUZHOU- CONTRACT MFR) |
Source: openFDA. Public-domain (CC0).