FDA device listing
TIVA 2 &, TIVA 8,TIVA 2 &, TIVA 8, TIVA 10
FDA device listing 2011056900 · TUTTNAUER LTD.
Key facts
| Proprietary names | TIVA 2 &, TIVA 8,TIVA 2 &, TIVA 8, TIVA 10 |
|---|---|
| Owner/operator | TUTTNAUER LTD. |
| Owner/operator number | 8030087 |
| Product codes | LDS |
| Device names | LDS - Device, Pasteurization, Hot Water |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.6991 |
| Review panels | General Hospital |
| Registered establishments | TUTTNAUER LTD. |
| Establishment registrations | 8030087 |
| FEI numbers | 3005343391 |
| Establishment operations | 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