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Factors for devising a schedule for maintenance of autoclaves complying with Part 1 of BS 2646.
Guidance in relation to autoclaves for the sterilization of material and equipment, including make-safe loads, which may be contaminated with organisms categorized as Hazard Groups 1, 2 or 3.
4.1 Single-use systems (SUSs) used for biopharmaceutical manufacturing must maintain sterility and product quality of the fluid inside. Such articles or systems should therefore be validated as providing an effective barrier against microbial ingress. The microbial barrier properties of a SUS may...
3.1 The solubility of glass in contact with food, beverages, or pharmaceutical products is an important consideration for the safe packaging and storage of such materials. Autoclave conditions are specified since sterilization is often employed for the packaging of the product. It...
Use of autoclaves other than of material contaminated with Hazard Group 4 organisms.
This European Standard specifies performance criteria for the steam sterilizer and autoclave used for the destruction and prevention of release of microorganisms used in biotechnological processes.
Specifies requirements for the design, construction and performance of autoclaves operating with saturated steam at temperatures up to 138°C and pressure not exceeding 2.4 bar nominal and for operation under vacuum (subject to external pressure).
Describes methods of test used to verify compliance with the requirements for design, construction, safety and performance specified in BS 2646-1:1992.
Replacement: This standard applies to AUTOCLAVES and STERILIZERS, including those with an automatic loading and unloading system, which incorporate a CHAMBER using toxic gas intended for the treatment of medical materials, and for laboratory processes, for example for...
4.1 Single-use systems (SUSs) used for biopharmaceutical manufacturing must maintain sterility and product quality of the fluid inside. Such articles or systems should therefore be validated as providing an effective barrier against microbial ingress. The microbial barrier properties of a SUS may...
In dieser Norm wird ein Verfahren zur Bestimmung der Autoklaven-Sterilisi
The General Services Administration has authorized the use of this Commercial Item Description. This Commercial Item Description covers a disposable wrapper suitable for wrapping surgical supplies for sterilization by autoclaving.
Section I applies to several types of boilers and components of boilers, such as economizers, superheaters, reheaters, and in some circumstances feedwater heaters. Although its title is Power Boilers, the scope of Section I is somewhat broader. The Preamble to Section I explains that it covers...
3.1 The solubility of glass in contact with food, beverages, or pharmaceutical products is an important consideration for the safe packaging and storage of such materials. Autoclave conditions are specified since sterilization is often employed for the packaging of the product. It...
