FDA device listing
1000cc Suction Liner,1500cc Suction Liner,3000cc Suction Liner,SUCTION LINER & CANISTER
FDA device listing 1063239571 · Saferlife Products Co.,Ltd.
Key facts
| Proprietary names | 1000cc Suction Liner,1500cc Suction Liner,3000cc Suction Liner,SUCTION LINER & CANISTER |
|---|---|
| Owner/operator | Saferlife Products Co.,Ltd. |
| Owner/operator number | 10031800 |
| Product codes | KDQ |
| Device names | KDQ - Bottle, Collection, Vacuum |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.6740 |
| Review panels | General Hospital |
| Registered establishments | SAFERLIFE PRODUCTS CO.,LTD. |
| Establishment registrations | 3008264111 |
| FEI numbers | 3008264111 |
| Establishment operations | Manufacturer, Repackager/Relabeler |
| 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