FDA device listing
Ear Suction Tubes; Ear Suction Tube with Suction Controller; Suction Controller; Suction Handles; Fine ends
FDA device listing 1996909322 · Eon Meditech Pvt. Ltd.
Key facts
| Proprietary names | Ear Suction Tubes; Ear Suction Tube with Suction Controller; Suction Controller; Suction Handles; Fine ends |
|---|---|
| Owner/operator | Eon Meditech Pvt. Ltd. |
| Owner/operator number | 10085729 |
| Product codes | JZF |
| Device names | JZF - Tube, Ear Suction |
| Device class | Class I |
| Classification regulations (21 CFR) | 874.4420 |
| Review panels | Ear, Nose, & Throat |
| Registered establishments | EON MEDITECH PVT. LTD. |
| Establishment registrations | 3023464160 |
| FEI numbers | 3023464160 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| 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