0.4 Ml Mini Spore Ampoules

0.4 Ml Mini Spore Ampoules Specification

Height
Standard ampoule size

Suitable For
Autoclaves dry heat ethylene oxide and other sterilization processes

Treatment Type
Sterilization

Automation Grade
Manual usage

Application
Sterilization validation in medical and industrial environments

Weight
Lightweight

Phase
Solid

Function
To confirm sterility assurance levels

Temperature Range
Compatible with sterilization temperatures

Color Code
Purple

Shape
Cylindrical

Accuracy
High biological accuracy

Product Type
Mini Spore Ampoules

Use
Used for biological verification of sterilization processes

Material
Glass

Properties
High resistance Durable

About 0.4 Ml Mini Spore Ampoules

Being a leading exporter and supplier of different kinds of ampoules, we bring forth for our clients the 0.4 Ml Mini Spore Ampoules. In order to monitor the steam process, these products consist hermetically sealed glass ampule. Our provided products are available with modified Trypticase Soy Broth, a pH indicator and Geobacillus stearothermophilus with a population level of 106. In addition, these 0.4 Ml Mini Spore Ampoules save time by eliminating aseptic culturing.

Features:

Visually distinct positive results indicated by the media transitioning from Purple to Yellow
Negative controls are available separately
Come in various capacities

Technical Specifications

Crosstex Code	OS1-50-06
Volume	0.4 ml
Shelf Life	24 Months
Packaging Type	Box

Reliable Sterilization Validation

Our 0.4 ml Mini Spore Ampoules are engineered to provide high biological accuracy when confirming the effectiveness of sterilization processes. The glass ampoules' robust material withstands harsh sterilization environments, ensuring consistent performance during routine validation or process qualification.

Versatile Across Sterilization Methods

These ampoules are compatible with various sterilization methods, such as autoclaves, dry heat, and ethylene oxide, making them suitable for multiple applications. Whether used in healthcare, laboratories, or industrial settings, they offer dependable results for regulatory compliance and safety assurance.

FAQ's of 0.4 Ml Mini Spore Ampoules:

Q: How are the 0.4 ml Mini Spore Ampoules used in sterilization validation processes?

A: The ampoules are placed inside sterilization chambers alongside items being treated. After the process, they are incubated to verify if any spores survived, providing a biological confirmation of the sterilization cycle's effectiveness.

Q: What benefits do these Mini Spore Ampoules offer over traditional indicators?

A: They offer high biological accuracy, rapid results, and resistance to different sterilization methods. Their glass construction ensures durability, while their small size allows for versatile application in tight or varied spaces.

Q: When should these ampoules be used during the sterilization process?

A: These ampoules are typically used during routine sterilizer validation, process qualification, or when verifying sterility assurance levels, especially in new or adjusted sterilization cycles.

Q: Where can these ampoules be applied for sterilization validation?

A: The ampoules are suitable for use in medical, pharmaceutical, and industrial environments where reliable sterilization validation is required, particularly within India from suppliers and traders.

Q: What is the process for interpreting results from the ampoules?

A: After exposure and incubation, a color change or lack of microbial growth indicates successful sterilization. The high accuracy of these ampoules ensures reliable, clear results.

Q: How does the purple color code assist users?

A: The purple color code helps users quickly distinguish these ampoules from others, reducing errors and streamlining identification during intense sterilization and validation workflows.

Q: What is the main benefit of using manual 0.4 ml Mini Spore Ampoules for sterility assurance?

A: Manual usage allows for flexible placement and retrieval in diverse equipment, ensuring comprehensive validation and adaptability to unique testing requirements.

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