FDA device listing
Duodenoscope And Accessories, Flexible/Rigid
FDA device listing 1951362326 · MIC International
Key facts
| Owner/operator | MIC International |
|---|---|
| Owner/operator number | 10087043 |
| Product codes | FDT |
| Device names | FDT - Duodenoscope And Accessories, Flexible/Rigid |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.1500 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Yoshikawa Kasei Co., Ltd. Medical Company Osaka Plant, Yoshikawa Kasei Co., Ltd. Medical Company Shizuoka Plant |
| Establishment registrations | 3004638277, 3014055212 |
| FEI numbers | 3004638277, 3014055212 |
| Establishment operations | Contract 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