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Reference: 802B-CSADXSXD4 SER A
Brand: Allen-Bradley (Rockwell Automation)
Allen-Bradley 802B-CSADXSXD4 SER A Compact Limit Switch
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Reference: 00036672
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Distek 2100 Dissolution System
The Distek 2100 Dissolution System is a versatile and reliable instrument designed for the dissolution testing of pharmaceutical dosage forms, such as tablets and capsules. It facilitates the measurement of the rate at which active pharmaceutical ingredients dissolve in a specified medium, ensuring compliance with industry standards and aiding in quality control and research applications.
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90-days money back guarantee
Description
The Distek 2100 series, including models like the 2100A, 2100B, and 2100C, offers flexibility and configurability to meet diverse dissolution testing requirements. These systems are equipped with user-friendly interfaces, precise control mechanisms, and robust construction to ensure accurate and repeatable results. The 2100C model, for instance, features a compact design with space-saving elements and productivity-enhancing features, maintaining its position at the forefront of traditional bath-based dissolution systems.
Features:
- Accommodates up to 8 vessels ranging in size from 100 mL to 4 liters, allowing a wide range of tests to be conducted on the same unit.
- USP-compliant interchangeable stirring devices with a "quick-change" height adjustment spacer for rapid transitions between different apparatus types without removing the shaft.
- Integrated thermocirculator with a vertical design that can be positioned behind the bath, requiring no additional bench space.
- User-friendly touch screen interface for intuitive operation and method management.
- Extensive reporting and method storage capabilities for comprehensive data management.
Product Details
2100 Series
1 Item
New
Specific References
- MPN
- 2100
The Distek 2100 Dissolution System is a versatile and reliable instrument designed for the dissolution testing of pharmaceutical dosage forms, such as tablets and capsules. It facilitates the measurement of the rate at which active pharmaceutical ingredients dissolve in a specified medium, ensuring compliance with industry standards and aiding in quality control and research applications.