FDA device listing
UNIT, SYRINGE, AIR ANDIOR WATER
FDA device listing 1188644425 · Shandong Zhushi Pharmaceutical Group Co., Ltd
Key facts
| Proprietary names | UNIT, SYRINGE, AIR ANDIOR WATER |
|---|---|
| Owner/operator | Shandong Zhushi Pharmaceutical Group Co., Ltd |
| Owner/operator number | 10052646 |
| Product codes | ECB |
| Device names | ECB - Unit, Syringe, Air And/Or Water |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.4565 |
| Review panels | Dental |
| Registered establishments | SHANDONG ZHUSHI PHARMACEUTICAL GROUP CO., LTD |
| Establishment registrations | 3013496867 |
| FEI numbers | 3013496867 |
| 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