FDA device listing
Disposable nitrile glovcs;Disposablelatex gloves; Disposable PVC gloves; Disposable mixed Ding gloves
FDA device listing 1304999673 · Minlong Pharmaceutical Biotechnology (Shenzhen) Co., Ltd
Key facts
| Proprietary names | Disposable nitrile glovcs;Disposablelatex gloves; Disposable PVC gloves; Disposable mixed Ding gloves |
|---|---|
| Owner/operator | Minlong Pharmaceutical Biotechnology (Shenzhen) Co., Ltd |
| Owner/operator number | 10090805 |
| Product codes | PXC |
| Device names | PXC - Personal Protection Kit |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6250 |
| Review panels | General Hospital |
| Registered establishments | Minlong Pharmaceutical Biotechnology (Shenzhen) Co., Ltd. |
| Establishment registrations | 3031590640 |
| FEI numbers | 3031590640 |
| 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