RADWAG PS 600.5Y PS 5Y Precision Balance, 600g Capacity, 1mg Readability, 21 CFR Part 11, Internal Calibration
RADWAG PS 600.5Y Precision Balance — 21 CFR Part 11 Ready with 1 mg Resolution
Pharmaceutical and biotech laboratories operating under FDA oversight need weighing instruments that support electronic record compliance from day one. The RADWAG PS 600.5Y Precision Balance provides 600 g capacity at 1 mg readability with built-in 21 CFR Part 11 features, automatic internal calibration, and a 10-inch touchscreen equipped with customizable widgets and the ReflexLEVEL automatic levelling system.
Key Features
- 21 CFR Part 11 Compliance: Electronic signatures, user access controls, and comprehensive audit trails satisfy FDA requirements for electronic records in validated environments.
- 600 g Capacity at 1 mg Readability: Fine resolution on a mid-range platform handles dispensing, formulation, and analytical preparation tasks with confidence.
- Automatic Internal Calibration: Runs on schedule or in response to environmental shifts, ensuring measurement integrity with full GLP documentation.
- ReflexLEVEL Automatic Levelling: Motorized levelling corrects instrument orientation automatically, removing a common source of measurement error from daily operations.
- 10-Inch Touchscreen with Widgets: Real-time data widgets, process statistics, and customizable layouts put essential information at the operator's fingertips.
Detailed Overview
The PS 600.5Y delivers linearity of ±3 mg and standard repeatability of 0.5 mg at 5 % load, ensuring reliable performance across the full capacity. Part of the RADWAG PS 5Y series, it supports semi-automatic LevelSENSING alongside the motorized ReflexLEVEL system for dual-layer levelling assurance. Connectivity options include USB-A, USB-C, Ethernet, Wi-Fi, and Hotspot, facilitating validated data transfer to LIMS, ERP, or networked archival systems. The built-in database engine manages user profiles, product records, and standard operating procedures directly on the balance, minimizing reliance on external documentation during regulated weighing operations.
Applications
- Pharmaceutical dispensing and formulation under GMP
- Biotech sample preparation with validated data recording
- Clinical trial material weighing and documentation
- Regulated chemical production with audit trail requirements
Why Choose this precision balance?
The PS 600.5Y removes the compliance burden from your weighing process by embedding 21 CFR Part 11 functionality directly into the balance. With automatic calibration, automatic levelling, and a powerful touchscreen interface, it lets your team focus on science rather than paperwork. Add to cart and bring validated precision to your regulated laboratory.
| Maximum Capacity | 600 g |
|---|---|
| Readability | 1 mg |
| Tare range | -600 g |
| Standard repeatability [5% Max] | 0.5 mg |
| Standard repeatability [Max] | 1.5 mg |
| Standard minimum weight (USP) | 1 g |
| Standard minimum weight (U=1%, k=2) | 0.1 g |
| Linearity | ±3 mg |
| Stabilization time | 2 s |
| Calibration | internal (automatic) |
| Leveling system | semi-automatic - LevelSENSING |
| Weighing pan dimensions | 128×128 mm |
| Display | 10″ touchscreen |
| Communication interface | USB-A ×2, USB-C, HDMI, Ethernet, Wi-Fi®, Hotspot |
| Database capacity | 7 |
| Protection class | IP 43 |
| Operating temperature | +10 — +40 °C |
| Power supply | Adapter: 100 – 240V AC 50/60Hz 0.6A; 12V DC 1.2A Waga: 12 – 15V DC 0.8A max |
| Power consumption | 4 W |
| Net weight | 3.99 kg |
| Touch-free operation | 2 IR Sensors |
| Ambient conditions monitoring | THBR 2.0 System, THBR BOX, THB P, THB W, THB S |
| Relative humidity | 40% — 80% |
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