Thermo Scientific Chromeleon7 CDS 7.1 SR3 with License Dongle and File Disk

Thermo Scientific Chromeleon 7.1 SR3 Chromatography Data System (CDS). This enterprise-grade analytical software platform provides centralized instrument control, high-throughput data acquisition, and automated processing for chromatography and mass spectrometry systems. The provided physical installation kit utilizes a cryptographically secured USB hardware dongle to authenticate local or client-server sessions, ensuring continuous operational uptime and strict regulatory data integrity across analytical workflows.

• MPN / Catalog Model: Chromeleon 7.1 SR3 (Specific sub-SKUs vary based on instrument class licenses, e.g., Single Edition or Enterprise).
• Manufacturer & Line: Thermo Scientific (software division formerly originating from Dionex, now integrated under Thermo Fisher Scientific).
• Quantity & Packaging / Form Factor: Single software deployment kit consisting of physical installation media (CD/DVD-ROM file disk) and one (1) USB hardware security key (dongle).
• Material Construction / Metallurgy: Physical deliverables consist of a standard polycarbonate optical disk and a robust USB Type-A hardware key containing an internal EEPROM cryptographic chip for secure, offline license storage.
• Technical Specifications & Tolerances: Represents Chromeleon Version 7.1, Service Release 3 (SR3). Operates on a relational database architecture utilizing secure Data Vaults (SQL Server or Oracle-based). The dongle mandates a continuous 5V USB connection to validate active instrument controllers and client interfaces, maintaining processing authorization without requiring an active internet connection or centralized network license server.
• Hardware & System Compatibility: Provides native driver integration for Thermo Scientific LC, GC, IC, and MS platforms (such as Dionex ICS, Trace GC, and UltiMate series), as well as extensive third-party analytical instrumentation via RS-232, GPIB, and TCP/IP Ethernet communication protocols.
• Standards, Cleanliness & Purity: Architecture is explicitly designed for GxP and cGMP validated environments, providing full compliance frameworks for FDA 21 CFR Part 11 regulations through comprehensive access controls, electronic signatures, and unalterable relational database audit trails.
• Primary Application: Routine quantitative analysis, QA/QC batch processing, and method development in analytical chemistry laboratories utilizing High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ion Chromatography (IC), and Mass Spectrometry (MS).

Includes Software disk, manual, serial disk, and serial key. Serial Disk and Serial Key numbers DO NOT match.