FDA device listing
CABLE, TRANSDUCER AND ELECTRODE, PATIENT
FDA device listing 1044613504 · SunMed Group Holdings, LLC dba AirLife
Key facts
| Proprietary names | CABLE, TRANSDUCER AND ELECTRODE, PATIENT |
|---|---|
| Owner/operator | SunMed Group Holdings, LLC dba AirLife |
| Owner/operator number | 10044795 |
| Premarket submissions | K163316 |
| Product codes | DSA |
| Device names | DSA - Cable, Transducer And Electrode, Patient, (Including Connector) |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.2900 |
| Review panels | Cardiovascular |
| Registered establishments | AirLife Finland Oy, SUNMED GROUP HOLDINGS, LLC dba AirLife |
| Establishment registrations | 3010838917, 3030308442 |
| FEI numbers | 3010838917, 3030308442 |
| Establishment operations | Complaint File Establishment, Specification Developer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 10–99 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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