Details
The device is not suitable for use on neonatal patients, pregnant women, patients with implanted,electronic devices, patients with pre-eclampsia, premature ventricular beats, atrial fibrillation,peripheral, arterial disease and patients undergoing intravascular therapy or arterio-venous shunt or people who received a mastectomy.
Additional Information
| Product Code | No |
|---|---|
| Bar Code | 5016870225318 |
| Height | No |
| Length | No |
| Diameter | No |
| Width | No |
| Brand | Kinetik |
| Size | No |
