You searched for: Sterilisation Indicators

Supplier: CROSSTEX

Spore suspensions are pure suspensions of viable spores from specific organisms of known resistance to various sterilisation processes. These biological indicators are used to validate that bacterial spores have been completely destroyed. The indicator is simply processed with the load in the steriliser. No bacterial growth after culturing indicates that the sterilisation process is effective. Growth indicates ineffective sterilisation.

Supplier: 3M MEDICAL

The 3M™ Comply™ Steam Chemical Indicator 1251 is a paper strip 1,5 cm wide by 20 cm long printed with a chemical indicator ink that turns from red to green when exposed to the steam sterilisation process.

Supplier: CROSSTEX

Spore discs are used to monitor the plasma/vaporised hydrogen peroxide sterilisation processes. Place the spore discs either directly into the chamber or positioned in areas of a device which are the most difficult to sterilise or distributed throughout rooms and isolators.

Supplier: DELTALAB

Sterilisation indicator tapes for steam autoclave.

Supplier: 3M MEDICAL

Biological indicators provide the best assurance of sterility by challenging the steriliser with quantifiable, highly resistant spores. After sterilisation, the vial is 'crushed' to join the growth media with the processed spore strip. A colour change to yellow indicates surviving spores and a positive result. Biological indicators are used for load control monitoring which is the process by which a load is monitored and released based on the result of a biological indicator (BI) in a test pack.

Supplier: S▄DPACK MEDICA

Tapes indicators by dry heat sterilisation.

Supplier: 3M MEDICAL

The Electronic Test System (ETS) is a stand alone test device for measurements of the physical parameters of a steam sterilisation cycle providing an accurate temperature, pressure and time measurement.

Supplier: 3M MEDICAL

The 3M Comply indicator tapes are an integral part of a coordinated sterilisation control system.

Supplier: CROSSTEX

Chemical process indicators provide a fast and consistent visual check on items that were sterilised by EO.

Supplier: CROSSTEX

Self-adhesive, non toxic, chemical process indicators change from blue to pink upon exposure to 10 minutes of saturated steam at 121 °C or 2 minutes at 134 °C. Longer exposure will result in a brighter shade of pink. The blue to pink colour transition is sensitive to time, temperature, and the presence of saturated steam.

Supplier: S▄DPACK MEDICA

The discs are available in a variety of blank or printed versions.

Supplier: CROSSTEX

Self-contained biological indicators (SCBIs) for monitoring steam sterilisation consist of a durable PC vial with cap, a crushable glass ampoule with Trypticase® soy broth (TSB) modified with pH indicator, and a disc inoculated with Geobacillus stearothermophilus spores.

Supplier: 3M MEDICAL

Twenty four minute Biological Indicator Challenge Pack for 132°C (270°F) 4 minute and 135°C (275°F) 3 minute Dynamic Air Removal Steam Sterilization. Each pack contains one 3M™ Attest™ Super Rapid Readout Biological Indicator 1492V.

Supplier: CROSSTEX

These spore ampoules are ideal for use in validation and routine monitoring of liquid steam sterilization cycles. Spore ampoules are manufactured using hermetically sealed Type I borosilicate glass containing an exclusively formulated Tryptic
Soy Broth (TSB) modified with pH indicator, and Geobacillus stearothermophilus spores. No activation is required; simply expose Spore Ampoules to sterilization process and incubate.

Supplier: 3M MEDICAL

Internal pack monitor for use with Vaporised Hydrogen Peroxide/Gas Plasma sterilisation processes.

Supplier: CROSSTEX

Spore coupons for use in monitoring plasma/vapourised hydrogen peroxide (VH₂O₂) sterilisation processes.

Supplier: 3M MEDICAL

3M™ Attest™ Super rapid readout biological indicators and challenge packs for steam, super rapid 1-hour results.

Supplier: CROSSTEX

Bacillus subtilis strips for monitoring low temperature steam sterilisation processes.

Supplier: CROSSTEX

Self-adhesive, non-toxic, chemical process indicators that change from yellow to red upon exposure to gamma or electron beam radiation. Labels are coated with a UV blocking agent for protection from exposure to UV light. A minimum of 15 kGy irradiation is recommended for sufficient end-point colour development. At greater dosage levels, the radiation indicators exhibit a darker shade of red.

Supplier: 3M MEDICAL

This auto-reader for steam, 390, is designed to incubate and automatically read the biological indicators for steam at 60 °C for a final fluorescent result.

Supplier: CROSSTEX

Inoculated carrier mini spore discs for monitoring EO and dry heat processes.

Supplier: CROSSTEX

Biological sterilisation discs are used to perform sterilisation cycle validation in small areas of a device, where a standard-sized spore strip will not fit, such as within a syringe barrel, inside tubing, or under a cap. Spore discs are created by inoculating spore suspensions of certified population and resistance onto paper discs.

Supplier: CROSSTEX

CPI-DP1 are intended for use with individual units (e.g. packs, containers) to indicate that the unit has been directly exposed to a high temperature dry heat or depyrogentation process and to distinguish between processed and unprocessed units.

Supplier: 3M MEDICAL

With unique colour chemistry, the 3M™ Comply™ Disposable Bowie and Dick Type Autoclave Test Pack has been designed for single use in porous load sterilizers for daily Bowie and Dick tests.

Supplier: 3M MEDICAL

The Bowie and Dick test is carried out daily in an empty chamber after a warm up cycle and is designed to show the adequacy of steam penetration.

Supplier: 3M MEDICAL

Auto-reader for use with 3M™ Attest™ Rapid Readout Biological Indicators and process challenge packs for steam. Includes ethernet cable for web app connectivity.

Supplier: 3M MEDICAL

The 3M™ Attest™ Vaporized Hydrogen Peroxide Tri-Metric Chemical Indicator 1348/1348E verifies that the stated values for the three critical parameters of exposure time, temperature, and amount of vaporized hydrogen peroxide have been achieved within a package or containment device (i.e. wrapped trays, rigid containers, sterilization pouches, and other types of packs) and/or at a specific location within the load or empty chamber.