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DCSmart
DCSmart is equipped with functions such as recipe version management, audit trail, batch management, electronic signature, and user management for modern pharma capping dispensing. The device connects wirelessly to the operator interface, enabling broader application environments. To ensure operational safety, a dual-trigger design is implemented. The system supports electronic batch report generation via Ethernet or USB, and provides real-time audit trails through Ethernet, enhancing traceability throughout the production process.
| Power Supply: 220V | Power: 0.6kW |
| Capacity: 420~600 vials/h | Cap Range: 8-33mm |
| Weight: 35Kg | Dimensions: 455mmx325mmx650mm（LxWxH) |
Designed specifically for sealing of pharmaceutical vials with aluminum caps or aluminum-plastic caps, ideal for modern pharma capping dispensing workflows.
The machine is specifically designed for pharmaceutical vials using aluminum caps or aluminum-plastic caps. It supports cap sizes ranging from 8 mm to 33 mm, making it suitable for various vial formats commonly used in sterile injectable production, biotechnology, and R&D applications.
DCSmart was developed specifically to improve sealing integrity while reducing common capping issues. Tailin states that its segmented torque crimping technology helps reduce aluminum particle generation and maintain stable sealing performance, even when aluminum caps are slightly deformed. The system is also designed to protect vials from exploding during the capping process.
Yes. DCSmart is constructed with full 316L stainless steel and is resistant to VH2O2/VHPS/VHP sterilization environments, making it suitable for pharmaceutical cleanrooms and aseptic processing areas. The wireless operation and digital control features also help reduce operator intervention inside controlled environments.
Yes. The system supports real-time audit trails, electronic batch report generation, and PDF export functions through Ethernet or USB connections. These features help manufacturers maintain detailed production records and improve overall process traceability for compliance and quality investigations.
The system includes alarm indication functions and user management controls to help operators identify abnormal conditions quickly. Combined with audit trails and electronic records, these functions support troubleshooting, accountability, and process security in regulated pharmaceutical environments.
