FDA device listing
Vessel Dilator For Percutaneous Catheterization
FDA device listing 1860648398 · TARYAG Sterilization and Laboratories Ltd.
Key facts
| Proprietary names | Vessel Dilator For Percutaneous Catheterization |
|---|---|
| Owner/operator | TARYAG Sterilization and Laboratories Ltd. |
| Owner/operator number | 10050393 |
| Product codes | DRE |
| Device names | DRE - Dilator, Vessel, For Percutaneous Catheterization |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.1310 |
| Review panels | Cardiovascular |
| Registered establishments | TARYAG Sterilization and Laboratories Ltd. |
| Establishment registrations | 3012453745 |
| FEI numbers | 3012453745 |
| Establishment operations | Contract Sterilizer |
| 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