AR7106 Recorder for Pharmaceutical Machinery
Batch management recorder for the pharmaceutical industry, compliant with FDA 21 data integrity requirements, supporting electronic signatures and three-level permission management.
- Original Factory Genuine, Tenfold Compensation for Counterfeits
- Full Machine Warranty, Lifetime Maintenance
- In Stock, Shipped on the Same Day
The AR7106 is a batch management recorder designed specifically for the pharmaceutical industry, featuring 6 analogue input channels, 3 pulse input channels, 2 analogue output channels and 16 DO relay output channels. The instrument uses a 7-inch touchscreen and supports universal analogue input and power distribution output.
The recorder complies with FDA 21 requirements, using electronic signatures instead of manual signatures for security and effectiveness; it features three-level hierarchical permission management, a proprietary encryption mode and batch data recording, enabling traceability and review of production line processes, and is suitable for pharmaceutical, biological product and other applications with strict data integrity requirements.
| Parameter Name | Technical Specifications |
|---|---|
| Channel configuration | |
| Analogue input | 6 channels |
| Analogue output | 2-channel |
| Digital input | 3-channel |
| Relay output | 16-channel |
| Frequency input | 3-channel |
| Time-proportional output | 8-channel |
| Signal input | |
| Current | 4～20mA, 0～20mA |
| Voltage | -10～10V, -100～100mV |
| Frequency | 0～10kHz (0～32V) |
| Thermistors | Pt100, JPt100, PT1000, Cu50 |
| Thermocouples | B, E, J, K, S, T, N, R, WRe5-26, WRe3-25, etc. |
| Digital | 0～32V |
| Accuracy and communication | |
| Sampling period | 0.5 s |
| Measurement accuracy | ±0.2% |
| Communication | RS232/RS485 and Ethernet |
| Data interface | USB flash drive |
| Power distribution specification | 200mA/24V |
| Isolation | 400VAC between channels; 1500VAC between channel and ground |
| Power supply and environment | |
| Power Supply | AC (100～240) V, (47～63) Hz |
| Power dissipation | ≤30VA |
| Operating Temperature | （-20～60）℃ |
| Relative Humidity | (5–95)%RH |
| Fuse specification | 250VAC/3A, slow-blow type |
| Data integrity | |
| Compliance | Complies with FDA 21 data integrity requirements for recorders |
| Permission management | Three-level hierarchical permission management; the highest level can assign operating permissions to lower levels |
| Electronic signature | Real-name operation; the operator is responsible for the operation performed |
| Storage encryption | Binary storage format + checksum encryption; data cannot be modified |
| Dimensions | |
| Dimensions | 191.5mm×159.5mm×195mm |
| Hole size | 138mm×138mm |
| Mounting panel thickness | (1.5–8.0)mm |
- Batch management recorder for the pharmaceutical industry, compliant with FDA 21 data integrity requirements
- Electronic signatures replace manual signatures; real-name operation with traceable responsibility
- Three-level hierarchical permission management; operating permissions can be assigned by role
- Batch data recording function, supporting product line process traceability and review
- Binary storage format with checksum encryption, ensuring data cannot be modified
- 6 analogue + 3 pulse inputs, 16 DO relay outputs
Pharmaceutical batch production records
Record temperature and pressure curves on sterilisation cabinets and reaction vessels, archive by batch and confirm with electronic signatures.
Clean area data traceability
Three-level permission management with encrypted storage, achieving tamper-proof production data and audit traceability.
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Need selection advice or bulk quotation?
Send us the working condition parameters (signal type, medium, range, pressure, temperature, connection method), and our engineers will provide a selection scheme and quotation within 1 working day.
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