FDA device listing
adapter with holder,Blood Collection Adapter,Blood Collection Device,Blood Collection Tube Holder,Blood Collection Tube…
FDA device listing 1777322481 · ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD
Key facts
| Proprietary names | adapter with holder,Blood Collection Adapter,Blood Collection Device,Blood Collection Tube Holder,Blood Collection Tube Holder WITH FEMALE LUER ADAPTER,Blood Collection Tube Holder WITH MALE LUER ADAPTER,Blood Collection Tube Holder with Safety Shield,Blood Culture Device,Blood Culture Device Female Luer Lock,Blood Culture Device Male Luer Lock,Blood Culture Transfer Holder With Female Luer… |
|---|---|
| Owner/operator | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
| Owner/operator number | 9036461 |
| Product codes | KST |
| Device names | KST - System, Blood Collection, Vacuum-Assisted, Manual |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.9125 |
| Review panels | Hematology |
| Registered establishments | ZHEJIANG KINDLY MEDICAL DEVICES CO., LTD |
| Establishment registrations | 9615588 |
| FEI numbers | 3003560965 |
| Establishment operations | Contract Manufacturer, 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