FDA device listing
FLAT DRAIN 13 mm - 103 713,FLAT DRAIN 2*5 mm - 103 705,FLAT DRAIN 3*7 mm - 103 707,FLAT DRAIN 4*10 mm - 103 710,ROUND…
FDA device listing 1678476638 · Plasti-med Plastik Medikal Urunler San. ve Tic. Ltd. Sti.
Key facts
| Proprietary names | FLAT DRAIN 13 mm - 103 713,FLAT DRAIN 2*5 mm - 103 705,FLAT DRAIN 3*7 mm - 103 707,FLAT DRAIN 4*10 mm - 103 710,ROUND SILICONE DRAIN 12 CH - 103 712,ROUND SILICONE DRAIN 15 CH - 103 715,ROUND SILICONE DRAIN 18 CH - 103 718,ROUND SILICONE DRAIN 21 CH - 103 721,ROUND SILICONE DRAIN 22 CH - 103 722,ROUND SILICONE DRAIN 24 CH - 103 724,ROUND SILICONE DRAIN 27 CH - 103 727,ROUND SILICONE DRAIN 30 CH… |
|---|---|
| Owner/operator | Plasti-med Plastik Medikal Urunler San. ve Tic. Ltd. Sti. |
| Owner/operator number | 10080023 |
| Product codes | GCD |
| Device names | GCD - Connector, Catheter |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4200 |
| Review panels | General & Plastic Surgery |
| Registered establishments | PLASTI-MED PLASTIK MEDIKAL URUNLER SAN. VE TIC. LTD. STI. |
| Establishment registrations | 3018762668 |
| FEI numbers | 3018762668 |
| Establishment operations | Foreign Exporter, 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