FDA device listing
Blood Collection and Infusion Set,Blood collection set,Safety blood collection set
FDA device listing 1292699484 · ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD
Key facts
| Proprietary names | Blood Collection and Infusion Set,Blood collection set,Safety blood collection set |
|---|---|
| Owner/operator | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
| Owner/operator number | 9036461 |
| Product codes | JKA |
| Device names | JKA - Tubes, Vials, Systems, Serum Separators, Blood Collection |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1675 |
| Review panels | Clinical Chemistry |
| Registered establishments | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
| Establishment registrations | 9615588 |
| FEI numbers | 3003560965 |
| Establishment operations | Contract Manufacturer, 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