FDA device listing
T2013 - Stirrup Boot Pads
FDA device listing 1032395363 · TECNOCIRURGICA COMERCIO DE MATERIAIS MEDICOS CIRURGICOS E HO
Key facts
| Proprietary names | T2013 - Stirrup Boot Pads |
|---|---|
| Owner/operator | TECNOCIRURGICA COMERCIO DE MATERIAIS MEDICOS CIRURGICOS E HO |
| Owner/operator number | 10094861 |
| Product codes | JEA |
| Device names | JEA - Table, Surgical With Orthopedic Accessories, Ac-Powered |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4960 |
| Review panels | General & Plastic Surgery |
| Registered establishments | TECNOCIRURGICA COMERCIO DE MATERIAIS MEDICOS CIRURGICOS E HOSPITALARES LTDA |
| Establishment registrations | 3043007473 |
| FEI numbers | 3043007473 |
| Establishment operations | 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