Import Em-301 — Buy in Bulk from Supplier in China

The EM-301 is a 12-lead electrocardiograph machine designed for clinical use in hospitals and outpatient clinics. It features an 80mm thermal printer for immediate 3-lead output and a 7-inch LCD screen with 800 x 480 pixel resolution to display all 12 leads simultaneously. The device captures and processes cardiac electrical signals with digital filtering to reduce noise from muscle tremor or power interference.

The machine operates on standard 100 - 240V AC input and includes built-in battery backup for portable use. Its compact, lightweight design allows for easy transport between wards or mobile clinics. The software supports standard ECG interpretation formats and outputs data in DICOM and PDF formats for integration with hospital information systems. The printer uses thermal paper rolls of standard 80mm width, compatible with common medical-grade consumables.

This device is commonly purchased by private clinics, rural health centers, and diagnostic labs in Southeast Asia and Africa seeking affordable, reliable cardiac monitoring. Buyers typically order in quantities of 5 to 20 units, with packaging in foam-lined cardboard cases. Trade terms are negotiated directly; common arrangements include FOB Shenzhen or CIF destination ports. Lead time is usually 15 to 25 days after order confirmation.

Shenzhen ECGMAC Medical Electronics Co.,Ltd is a registered medical device manufacturer based in Baoan District, Shenzhen. The company specializes in producing portable diagnostic equipment including ECG, EEG, and vital signs monitors. The listing indicates no published ISO 13485 certification, no clinical validation reports, and no export history visible in public records.

The supplier’s trust tier is 'harbor' and response metrics are unavailable, suggesting limited buyer engagement. While the company name appears in Chinese business registries, no verified factory audit reports or product registration numbers are provided. Buyers should request FDA 510(k) or CE Mark documentation before import. The supplier does not disclose production volume, R&D capacity, or clinical testing partners.