MODEL: DR-8M
The Reinheldt DR-8M Next Generation Manual Syringe Dissolution System is a premium German-engineered 8-station dissolution testing platform designed for pharmaceutical quality control, method development, and research laboratories. The system combines the simplicity of manual sampling with the precision of a syringe manifold, delivering highly accurate and reproducible dissolution testing. Its unique programmable variable dilution capability allows different aliquot volumes at each sampling interval, making it an ideal solution for complex dissolution profiles and advanced analytical methods. The DR-8M fully complies with USP, IP, Ph. Eur., and JP pharmacopeial requirements while offering secure data management and 21 CFR Part 11-ready features for regulated laboratories.
| Model | Reinheldt DR-8M Next Generation |
| Manufacturer | Reinheldt GmbH, Germany |
| System Type | Manual Syringe Dissolution System |
| Stations | 8 |
| Sampling Method | Manual syringe manifold |
| Unique Feature | Programmable variable dilution with different aliquot volumes for each sampling interval |
| Compliance | USP, IP, Ph. Eur., and JP Pharmacopeia |
| Display | 7-inch TFT color touchscreen |
| User Capacity | Up to 250 users with multi-level password protection |
| Data Storage | Up to 1000 product methods and 50,000 test reports |
| Sampling Program | Up to 24 programmable sampling intervals |
| Temperature Control | Independent digital controller with vibration-free circulation pump |
| Water Bath | Clear molded acrylic bath with bottom drainage |
| Lift Mechanism | Vibration-free motorized lift |
| Vessel Alignment | High-precision vessel centering with snap-fit shaft locking |
| Automatic Stirrer Height | USP Apparatus 1, 2, 5 & 6 |
| Connectivity | LAN, FTP backup, PDF report export |
| Data Integrity | Electronic Logbook, Audit Trail, Role-based User Access |
| Regulatory Compliance | 21 CFR Part 11 ready |
| Power Protection | Auto-resume after power interruption |

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