FDA device listing
1.5m Adult, Reusable, Hytrel, Bag Tube, with 22 Male Connector,Adult (22mm) Single limb corrugated + 3 Way exhalation…
FDA device listing 1176959549 · VINCENT MEDICAL MANUFACTURING. CO., LTD.
Key facts
| Proprietary names | 1.5m Adult, Reusable, Hytrel, Bag Tube, with 22 Male Connector,Adult (22mm) Single limb corrugated + 3 Way exhalation valve (VM version),Adult (22mm) Single limb Smoothbore + 3 Way exhalation valve (VM version),BAG TUBE, ADULT, REUSABLE, HYTREL, 1.5m,Inpsired Medical Adult Anaesthesia Breathing System including drapable/expandable tubing, connectors, spare limb,Inpsired Medical Prediatric… |
|---|---|
| Owner/operator | VINCENT MEDICAL MANUFACTURING. CO., LTD. |
| Owner/operator number | 10041038 |
| Product codes | CAI |
| Device names | CAI - Circuit, Breathing (W Connector, Adaptor, Y Piece) |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5240 |
| Review panels | Anesthesiology |
| Registered establishments | VINCENT MEDICAL MANUFACTURING. CO., LTD. |
| Establishment registrations | 1000604079 |
| FEI numbers | 1000604079 |
| Establishment operations | Foreign Exporter |
| 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