FDA device listing
Biliary Plastic Stent,Biliary Plastic Stent Introducer,Biliary Plastic Stent Introducer/ short-wire compatible,Biliary…
FDA device listing 1486069441 · Micro-Tech (Nanjing) Co., Ltd.
Key facts
| Proprietary names | Biliary Plastic Stent,Biliary Plastic Stent Introducer,Biliary Plastic Stent Introducer/ short-wire compatible,Biliary Plastic Stent Set,Biliary Plastic Stent Set/ short-wire compatible |
|---|---|
| Owner/operator | Micro-Tech (Nanjing) Co., Ltd. |
| Owner/operator number | 9067602 |
| Premarket submissions | K230127 |
| Product codes | FGE |
| Device names | FGE - Stents, Drains And Dilators For The Biliary Ducts |
| Device class | Class II |
| Classification regulations (21 CFR) | 876.5010 |
| Review panels | Gastroenterology & Urology |
| Registered establishments | Micro-Tech (Nanjing) Co., Ltd. |
| Establishment registrations | 3004837686, 3013440400 |
| FEI numbers | 3004837686, 3013440400 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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