FDA device listing
Mira Max Wand,Mira Plus Wand,Mira Ultra4 Wand
FDA device listing 1050047009 · Quanovate Tech Inc.
Key facts
| Proprietary names | Mira Max Wand,Mira Plus Wand,Mira Ultra4 Wand |
|---|---|
| Owner/operator | Quanovate Tech Inc. |
| Owner/operator number | 10054431 |
| Product codes | NGE |
| Device names | NGE - Test, Luteinizing Hormone (Lh), Over The Counter |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.1485 |
| Review panels | Clinical Chemistry |
| Registered establishments | QUANOVATE TECH INC. |
| Establishment registrations | 3013501873 |
| FEI numbers | 3013501873 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database