FDA device listing
filter pad(mattress insole),Nonwoven Fabric (PP, Spunlace,Wood Pulp Based),,Snus/Nootropic/Nicotine pouches Nonwoven…
FDA device listing 1971642450 · GUANGZHOU HUIMING FIBRE PRODUCTS CO., LTD.
Key facts
| Proprietary names | filter pad(mattress insole),Nonwoven Fabric (PP, Spunlace,Wood Pulp Based),,Snus/Nootropic/Nicotine pouches Nonwoven Cloth (Fabric),suitable for disposable mattress pads, disposable insoles, and food & liquid filtration applications |
|---|---|
| Owner/operator | GUANGZHOU HUIMING FIBRE PRODUCTS CO., LTD. |
| Owner/operator number | 10093160 |
| Product codes | JRL |
| Device names | JRL - Unit, Filter, Membrane |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | GUANGZHOU HUIMING FIBRE PRODUCTS CO., LTD. |
| Establishment registrations | 3038200636 |
| FEI numbers | 3038200636 |
| 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