Maximum flexibility

Published: 9-Feb-2004


A heat sterilising incubator that ensures constant contamination control with the flexibility of two decontamination cycles in one unit is the latest addition to Triple Red's range of laboratory products. The Nuaire-5510E offers two cycles for periodic heat sterilisation and cleaning and eradication of contaminating agents. These are a 95?C humidified decontamination programme with a complete cycle taking 14 hours to run and a 145?C high temperature dry decontamination cycle which takes 10 hours to complete. The chamber design allows for shorter heat up and cool down cycles and includes easily removable inner chamber plenum, gaskets, shelves and brackets for sterilisation in an autoclave. All Nuaire incubators have large HEPA filters which continually clean and distribute air within the chamber to Class 100 air quality within five minutes of door opening.

T: +44(0)1844 218322 sales@triplered.com

See more

You may also like

Analysis

The case for a facility monitoring system

Read more
In regulated manufacturing, monitoring environmental conditions and critical equipment is essential to protect product quality, yield, and patient safety. Facilities often use a Facility Monitoring System (FMS) to track factors like airborne particles, temperature, and humidity. Beyond regulatory compliance, FMS delivers real business value through reduced waste, improved yield, higher quality, and greater profitability

Trending Articles

  1. AdvanceTEC drives cleanroom innovation & growth with acquisition by Equans Leveraging scale, global reach, technology, prefabrication & modularisation
  2. Medicinal cannabis production with GMP-compliant cleanroom solutions Controlled environments are supporting quality, safety and regulatory compliance in cannabis manufacturing
  3. You need to be a subscriber to read this article.
    Click here to find out more.
    President Trump signs order for “regulatory relief” for domestic pharmaceutical manufacturers The US President has signed an executive order to direct the FDA to review current regulatory procedures, such as by reducing inspection frequency
  4. Pharmaceutical carbon reduction expert EECO2 achieves B Corp status A relatively unique certification in the cleanroom design industry, EECO2 has been determined to meet the necessary high standards of social and environmental performance, transparency, and accountability for B Corporation status
  5. You need to be a subscriber to read this article.
    Click here to find out more.
    Integrating “high-voltage leak detection” into automated visual inspection Leoni Ransmann and Jan Sende from Syntegon Technology talk about visual inspection of product containers like ampoules, which has been the industry standard for decades, and compare it to modern methods being emphasised in documents like the new EU GMP Annex 1

Upcoming event

Cleanzone Middle East

September 18-19 2025 | Conference | Conrad Dubai, United Arab Emirates See all

You may also like

Analysis

The case for a facility monitoring system

In regulated manufacturing, monitoring environmental conditions and critical equipment is essential to protect product quality, yield, and patient safety. Facilities often use a Facility Monitoring System (FMS) to track factors like airborne particles, temperature, and humidity. Beyond regulatory compliance, FMS delivers real business value through reduced waste, improved yield, higher quality, and greater profitability
Pharmaceutical

300 hours of performance with APSPG-Max

NewAge Industries, Inc., parent company of the AdvantaPure™ line of tubing, hose and quality accessories for the high-purity market, announces the launch of its’ newest line of tubing, AdvantaSil APSPG-Max silicone pump tubing
Design & Build

Kemtile to showcase single source flooring solutions at PPMA 2025

Kemtile is using PPMA 2025 to engage prospective customers on the benefits of coming to an internationally-backed industrial flooring and drainage business with a single source approach to flooring projects across the process and packaging industry
Pharmaceutical

Steriline at CPHI 2025

Flexibility, robotics and customisation for a zero loss approach
Design & Build

AdvanceTEC drives cleanroom innovation & growth with acquisition by Equans

Leveraging scale, global reach, technology, prefabrication & modularisation
Pharmaceutical

Steriline at Pharma Pro&Pack Expo 2025

With its own branch already established in India, Steriline confirms the importance of the Indian and of Asian markets in general for its growth and development
Design & Build

Preserve and protect your cleanroom with a Guardtech Group Cleanroom Service Plan

Suffolk-based construction experts offering elite packages to ensure all service, maintenance and decontamination needs are taken care of
Subscribe now