Wired Temperature Validation System

  • group nameValidation Device

  • Min Order1 piece

  • brand nameAIKSMED Steam Autoclave Sterilizer Manufacturer

  • modelQT-3200, QT-3400,QT-6000 Series

  • payment methodL/C, T/T

  • update timeSat, 08 Aug 2026 00:37:22 GMT

Paramtents

  • Model QT-3200

  • Offline validation with independent data storage

  • Number of probes 1~64 thermocouple probes (quantity optional, supports T-type and K-type)

  • Moisture heat probe range -100℃~150℃

  • Dry heat probe range 0℃~350℃

  • Corrected accuracy ±0.1℃

  • Touch screen 5.7-inch color touchscreen LCD

Packging & Delivery

  • Size56cm x36cm x30cm

  • Min Order1 piece

Briefing

The temperature validation instrument is available in wired versions, independently developed by AIKSMED over many years. It meets GMP requirements for data acquisition and analysis in validation work and is specifically designed to meet the high standards of validation for pharmaceutical, freeze-drying, biotechnology, medical device, and food industries. Ensuring high precision, it can perform validations on heat distribution performance, heat penetration performance, steam sterilization, dry heat sterilization, constant temperature and humidity incubator, cold storage, rotary sterilizer, ETO sterilizer, warehouses, etc.

Detailed

Temperature Validation System

The AIKSMED Temperature Validation System is a professional solution designed for temperature distribution and penetration validation in pharmaceutical, biotechnology, medical device, and food industries.

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Available in wired versions, the system provides accurate temperature data acquisition, analysis, and reporting for validation processes including steam sterilization, dry heat sterilization, freeze dryers, incubators, cold storage, and other temperature-controlled equipment.

The system consists of a validation instrument, monitoring software, and high-precision thermocouples. It enables users to perform qualification studies, generate validation reports, and maintain reliable validation records in compliance with GMP requirements.

The software supports electronic data management and complies with FDA 21 CFR Part 11 requirements for electronic records and data integrity.

High-Precision Temperature Measurement
>Supports 1–64 thermocouple channels
>Temperature resolution up to 0.01℃
>Corrected accuracy: ±0.1℃
>Supports T-type and K-type thermocouples

Flexible Validation Solution
>Supports wired and wireless validation configurations
>Suitable for laboratory, pharmaceutical, and industrial validation applications
>Complete solution including hardware, software, sensors, and accessories

Reliable Data Management
>Independent data storage capability
>Secure and traceable validation data
>Automatic validation report generation
>Data analysis and statistical calculation functions

GMP Compliance Software
>Complies with GMP requirements
>Supports FDA 21 CFR Part 11 electronic record requirements
>Provides IQ/OQ/PQ documentation support

Easy Operation
>User-friendly interface
>Stand-alone operation capability
>Real-time monitoring and data analysis


The AIKSMED Temperature Validation System is suitable for:

Sterilization Validation
>Steam sterilizers (Autoclaves)
>
Pulse vacuum sterilizers
>Dry heat sterilizers
>Ethylene oxide sterilizers (ETO)

Pharmaceutical Equipment Validation
>Freeze dryers / Lyophilizers
>
Stability chambers
>Incubators
>Cold storage equipment

Process Validation
>Heat distribution studies
>
Heat penetration studies

>F0 value calculation
>Temperature mapping

Validation Instrument

Parameter
Specification
Model
QT-3200 Series
Sensor Channels
1–64 thermocouple channels
Sensor Type
T-type / K-type thermocouple
Moist Heat Temperature Range
-100℃ ~ 150℃
Dry Heat Temperature Range
0℃ ~ 350℃
Accuracy
±0.1℃
Resolution
0.01℃
Sampling Frequency
1S
Data Storage Interval
5S ~ 240S
Communication Interface
TCP/IP
Input Voltage220V AC
Operating Temperature
-10℃ ~ 70℃
Operating Humidity
5%~95% RH (Non-condensing)
Display
5.7-inch color touchscreen LCD

Validation Software
>Automatic validation process management
>Online validation and offline data retrieval
>
Data analysis and statistical calculation

>Validation curve generation
>Electronic report generation
>
Audit trail and data traceability
>Lifetime free software upgrade 

Available validation documents:
>IQ (Installation Qualification)
>OQ (Operational Qualification)
>PQ (Performance Qualification)

Additional documents:
>User Manual
>Calibration Certificate
>Validation Report Template
>Software Operation Manual

6YRS JIANGSU AIKSMED EQUIPMENT CO., LTD

Nearest port for product export
Shanghai, China
Delivery clauses under the trade mode
FOB, CFR, CIF, EXW
Acceptable payment methods
T/T, L/C
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