FDA device listing
Crepe Paper, non-woven Fabrics, Composite non-woven Fabrics, Coated paper
FDA device listing 1569675770 · Anqing Kangmingna Packaging Co.,Ltd
Key facts
| Proprietary names | Crepe Paper, non-woven Fabrics, Composite non-woven Fabrics, Coated paper |
|---|---|
| Owner/operator | Anqing Kangmingna Packaging Co.,Ltd |
| Owner/operator number | 10059800 |
| Product codes | IME |
| Device names | IME - Pack, Hot Or Cold, Reusable |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5700 |
| Review panels | Physical Medicine |
| Registered establishments | ANQING KANGMINGNA PACKAGING CO.,LTD |
| Establishment registrations | 3008392711 |
| FEI numbers | 3008392711 |
| 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