OsmoTECH® PRO Multi-Sample Micro-Osmometer
Introducing our newest osmometer in our growing biotech focused portfolio. Designed specifically to fit your bioprocess needs, the OsmoTECH PRO delivers the highest level of data management, accuracy and precision, and ease-of-use available on the market today. The OsmoTECH PRO provides valuable concentration measurements while delivering unsurpassed data management capabilities, operational efficiency, ease of use, and features that support GMP, 21 CFR Part 11, and EU Annex 11 compliance. With its highly configurable settings, unparalleled operational efficiency, and robust data integrity features the OsmoTECH PRO can evolve with any of the changing needs of your organization. OsmoTECH PRO uses the proven freezing-point technology.
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Features
Effortlessly run multiple samples
Its 20 position turntable allows for walkaway testing.
Intuitive Touch-screen Interface
The menu-driven operating system, multi-language capability and touchscreen graphic interface all make for easy operation.
Small sample requirement
Just a 30 μL sample volume is needed for sample-limited applications.
Industry leading accuracy and precision
OsmoTECH PRO utilizes the Gold-standard testing method, freezing point depression to accurately and precisely determine osmolality.
Maintain traceability
The integrated barcode scanner helps with sample identification and reduces transcription errors.
Preserve your audit trail
Complete time-stamped record of usage, role, and actions requiring reason for settings changes. Unique ability to add comments to test results via the handy comments field.
Protect your data
Active Directory/LDAP options minimize manual input and the risk of errors, automatic or manual backups, 3 levels of user access, automatic logout timer keeps your data safe during idling – plus unlimited results and events storage
Easily integrate data management into your established workflow
Quickly save data to network database or USB or the embedded Web server and eliminate the need to manually manage date and time by synchronizing with network time.
Export data with ease
Do this in several ways including Open Protocol Communication (OPC), USB download, Network share, IS (TCP/IP communication), and an Optional DOT-MATRIX PRINTER.
OsmoTECH PRO is not for patient diagnostic use. Advanced Instruments certifies that the technical features needed for 21 CFR Part 11 compliance are built into OsmoTECH PRO. It is your responsibility to implement the necessary controls in your laboratory to comply with 21 CFR Part 11 requirements
Products & Supplies
Available Models
| OSMOTECH PRO | OsmoTECH PRO Instrument | |
Osmometer Calibration Standards and Reference Solutions
| SK-TECHPRO | Convenience Kit (Includes: 3MA029, 3MA005, 3MA085, 3MA200, 3LA028, 222825, 222840, 202850, 240821) | |
| 3MA029 | Clinitrol 290 Reference Solution, 10x2 mL Ampules | View |
| 3MA005 | 50 mOsm Calibration Standard, 10x2 mL | View |
| 3MA085 | 850 mOsm Calibration Standard, 10x2 mL | View |
| 3MA200 | 2000mOsm Calibration Standard, 10x2 mL Ampules | View |
| 3LA028 | Osmolality Linearity Set 100-2,000 mOsm 5x2x5 mL | View |
Supplies and Accessories
| 222825 | Disposable sample tubes | |
| 222840 | Probe wiper rings | |
| 202850 | Swab Cleaner Kit | |
| 240821 | Sampler Tips, 50/pkg | |
Accessories
| 135022 | Epson Dot Matrix Printer (sold-separately) | |
| AN2TP5 | Dot Matrix Printer Paper | |
Literature
| Brochure, OsmoTECH PRO | Download (PDF) |
Workflow Graphic
Testing osmolality is an essential parameter for process control and QC – just one of the many complex operational steps in biopharma manufacturing dedicated to producing a product of predetermined yield, purity and quality.
- Guarantee quality, potency and consistency during media development and raw material management.
- Monitor cell culture and fermentation to ensure optimal cell health, and consequently, high product quality and yield.
Ensure precise buffer preparation and prove complete buffer exchange to improve purification efficiency.
Safeguard your biologics as it passes through storage, reconstitution and injection.
Ensure that the final product meets your quality standards and release criteria.