FDA device listing
H12+ Holter Recorder
FDA device listing 1846668565 · BAXTER HEALTHCARE CORPORATION
Key facts
| Proprietary names | H12+ Holter Recorder |
|---|---|
| Owner/operator | BAXTER HEALTHCARE CORPORATION |
| Owner/operator number | 1417572 |
| Premarket submissions | K050896 |
| Product codes | DSH |
| Device names | DSH - Recorder, Magnetic Tape, Medical |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.2800 |
| Review panels | Cardiovascular |
| Registered establishments | WELCH ALLYN DE MEXICO, S. DE R.L. DE C.V., WELCH ALLYN, INC. |
| Establishment registrations | 1316463, 3006087789 |
| FEI numbers | 1316463, 3006087789 |
| Establishment operations | Contract Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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