Autoclave Temperature Data Loggers for Steam Sterilization

Consider the temperature range, accuracy (e.g., ±0.2°C), and physical durability. Ensure the logger is fully submersible (IP68 rated) to withstand steam and pressure. Also, verify it meets regulatory standards like FDA 21 CFR Part 11 for data integrity, which is critical for compliance.

Yes, our TempTrail™ series loggers are fully compliant with FDA 21 CFR Part 11. They generate secure, unalterable PDF and CSV reports with electronic signatures, ensuring complete data integrity and traceability for regulatory audits and quality assurance in the pharmaceutical and biotech industries.

Absolutely. Our autoclave data loggers are housed in a robust, sealed casing with an IP68 rating. This design ensures they are fully submersible and can withstand the high-pressure, high-temperature saturated steam environment typical of standard autoclave sterilization cycles, ensuring reliable performance run after run.

Data retrieval is simple and requires no special software. Just plug the logger into a USB port on any computer. It will automatically generate a secure, detailed PDF report and a CSV data file, which you can then save, print, or archive for your records.

No, one of the key advantages of our data loggers is that they are completely software-free. All configuration and report generation are handled directly by the device itself. This plug-and-play functionality eliminates software installation, validation, and maintenance, simplifying deployment and use.

The TempTrail™ HiTemp logger is designed for multiple uses and features a user-replaceable battery. This design reduces long-term operational costs and waste compared to single-use loggers. The long battery life ensures it can handle numerous sterilization cycles before needing a simple replacement.