FDA device listing
Denture Cup,Medicine Cup,Denture Cup,Stool Container
FDA device listing 2027460988 · ZHEJIANG MEDIUNION HEALTHCARE GROUP CO.,LTD
Key facts
| Proprietary names | Denture Cup,Medicine Cup,Denture Cup ,Stool Container |
|---|---|
| Owner/operator | ZHEJIANG MEDIUNION HEALTHCARE GROUP CO.,LTD |
| Owner/operator number | 9103599 |
| Product codes | KDT |
| Device names | KDT - Container, Specimen Mailer And Storage, Sterile |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.3250 |
| Review panels | Pathology |
| Registered establishments | ZHEJIANG MEDIUNION HEALTHCARE GROUP CO.,LTD |
| Establishment registrations | 3006210673 |
| FEI numbers | 3006210673 |
| 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