FDA device listing
Capilary Blood Collection Tubes 9NC Coagulation Sodium Citrate 3.2%;,Capilary Blood Collection Tubes 9NC Coagulation…
FDA device listing 1377219236 · ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD.
Key facts
| Proprietary names | Capilary Blood Collection Tubes 9NC Coagulation Sodium Citrate 3.2%;,Capilary Blood Collection Tubes 9NC Coagulation Sodium Citrate 3.8%,Capilary blood collection tube with clot activator and Gel;Capilary blood collection tube with EDTAK2;,Capilary blood collection tube with clot activator;Capilary blood collection tube no activator;,Capilary blood collection tube with EDTAK3;Capilary blood… |
|---|---|
| Owner/operator | ZHEJIANG GONGDONG MEDICAL TECHNOLOGY CO., LTD. |
| Owner/operator number | 9072045 |
| Product codes | GIO |
| Device names | GIO - Tube, Collection, Capillary Blood |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.6150 |
| Review panels | Hematology |
| Registered establishments | Zhejiang Gongdong Medical Technology Co., Ltd |
| Establishment registrations | 3005739529 |
| FEI numbers | 3005739529 |
| Establishment operations | 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