FDA Device Establishments · JSON-LD · Markdown
FEI 3018094310 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3018094310 |
|---|---|
| Owner / Operator | Medtronic, Inc. (#2112641) |
| Address | BSR Tech Park, Survey No.135, 138, 141 & 142 Nanakramguda Main Road, Hyderabad Telangana, 500032, IN |
| Mandatory US Agent | MEDTRONIC, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GEI |
| Regulation § (21 CFR) | 878.4400 |
| Proprietary names | Valleylab Flexible Argon Electrode Coagulation Only, E2530-3; Valleylab Argon Handset, E2520H; Valleylab Flexible Argon Electrode Coagulation Only, E2530-6; Valleylab Flexible Laparoscopic Argon Electrode Coagulation Only, E2530-28; Valleylab Argon Tungsten Sharp Needle Electrode, E2532 |
Source: openFDA. Public-domain (CC0).