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CleanSPOT Humidifiers

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GMP STANDARD. EU CE CERTIFIED.

Laboratory Humidity Control Systems

Unstable RH compromises sample integrity and can invalidate results before they're even analyzed.

CleanSPOT holds spec around the clock, EU CE certified and built for cleanroom classification.

Laboratory humidity control system for sample integrity
LABORATORY FACILITIES AT A GLANCE

What We Build For

Sample stability, equipment calibration, and cleanroom classification all depend on humidity staying within a defined range, continuously, not as an average across a working day.

RH precision
±1–2%
Standard
GMP
Certification
EU CE
Control integration
WiFi / BMS
Installation Qualification (IQ) and Operational Qualification (OQ) documentation available for facilities that require it as part of their own compliance program.

Why Humidity Control Matters in Laboratory Environments

Laboratories run on repeatability. Humidity drift introduces a variable that's hard to detect in the moment and hard to explain after the fact, when a result doesn't reproduce.

Sample and reagent stability

Hygroscopic samples and reagents absorb or lose moisture in response to ambient RH, which can shift concentration, weight, and behavior in ways that don't show up until testing is already underway. By then, the variable is baked into the result.

Equipment calibration drift

Sensitive instrumentation is often calibrated against a specific environmental baseline. Humidity swings outside that baseline can introduce measurement drift that's difficult to distinguish from genuine experimental variance.

Cleanroom classification tolerances

Labs operating under a formal cleanroom classification have a tighter environmental band to hold than a standard lab space. Humidification systems here need to hold spec tightly and predictably, not average out to the right number across a shift.

Reproducibility over time

A result that can't be reproduced under the same conditions is a real problem, and environmental drift is one of the quieter causes, since it's rarely the first thing investigated when a result doesn't match.

SYSTEMS FOR LABORATORY FACILITIES

Built for Sample Integrity

Precise, continuous control for spaces where a small drift has real consequences for your results.

WHY CLEANSPOT

Precision Equipment for Precision Work

Trusted by Research Institutions

Equipment supplied to IIBR Israel, among the research and clinical facilities that rely on our systems
We understand that a small environmental variable can be the difference between a reproducible result and a costly retest
Direct manufacturer, no distributor relaying your technical questions

Documentation Included

IQ/OQ documentation available for facilities that need proof equipment was installed correctly and performs to spec
EU CE certified, documentation ready for your own regulatory or accreditation file
Built to GMP standard from the start

Continuous, Not Spot-Checked

Full BMS integration, no standalone units creating a monitoring gap
±1–2% RH precision, held around the clock, not averaged across a shift
Built-in UVC LED disinfects the unit's own water supply continuously
COMPLIANCE

Meeting Your GMP Storage Requirements

Three standards, one integrated system, so you're not managing compliance for humidity control separately from everything else in your facility.

GMP standard

Systems built to GMP standards from the start, not retrofitted after the fact to meet requirements they weren't originally designed around.

VDI 6022

The German air hygiene standard for HVAC and humidification systems, covering hygienic design, maintenance, and inspection requirements for the equipment itself.

EU CE certified

Certified to essential EU requirements and standards, documented and available for your own regulatory file.
FAQ

Frequently Asked Questions

What RH precision can I expect? −
CleanSPOT's industrial ultrasonic humidifiers hold relative humidity within ±1–2%, continuously, not as a shift average.
Can these systems support cleanroom classification requirements? +
Yes, our systems are built to hold tight, predictable RH tolerances suited to classified cleanroom environments.
Do you provide documentation for accreditation or compliance files? +
Yes, IQ/OQ documentation is available, along with EU CE certification.
Have you supplied equipment to research institutions before? +
Yes, our equipment has been supplied to IIBR Israel among other research and clinical facilities.
Ready to Spec Your Laboratory?

Tell us your space and target RH, we'll recommend the right system.

Request a quote