FDA device listing
Biotronix Healthcare Pressary Remover
FDA device listing 1308750701 · Biotronix Healthcare Industries Inc.
Key facts
| Proprietary names | Biotronix Healthcare Pressary Remover |
|---|---|
| Owner/operator | Biotronix Healthcare Industries Inc. |
| Owner/operator number | 10043487 |
| Product codes | HHF |
| Device names | HHF - Remover, Intrauterine Device, Contraceptive, Hook-Type |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.4530 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | BIOTRONIX HEALTHCARE INDUSTRIES INC. |
| Establishment registrations | 3010131137 |
| FEI numbers | 3010131137 |
| Establishment operations | Repackager/Relabeler |
| 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