Krinmed · Sterilization monitoring, manufactured.info@krinmed.com
Krinmed
EEP Bowie-Dick Test Card
EEPManufacturer

EEP Bowie-Dick Test Card

Product overview

Designed for use in a compatible Bowie-Dick test system. The catalogue specifies 134°C with a 3.5-minute exposure. Select the associated components and test configuration according to the product instructions; the card is not an arbitrary substitute for a complete test pack.

Product specifications

Product code KRBD-118
Brand EEP
Manufacturer Krinmed
Indicator type 2
Dimensions, mm 50 × 90
Units per pack 30
Shelf life, months 48
Storage temperature 15–30°C
Listed test conditions 134°C / 3.5 min

Instructions for use

Select the cycle, placement and result interpretation according to this product’s instructions. A chemical indicator result alone does not establish sterility.

KRBD-118 is a test card for a compatible Bowie-Dick system, not an instruction to run a loose card in any chamber. Confirm the required surrounding components before use. Its catalogue lists a specific test condition, but compatibility also depends on the correct system configuration and sterilizer programme.

Where it fits in your workflow

Air removal testing addresses a different question from monitoring an individual instrument pack. It examines the test system response during a specified steam test cycle. This makes it useful in the equipment-checking workflow before routine processing, with the exact schedule governed by the applicable instructions and local procedure.

Practical use guide

Identify whether you are using a complete pack or a component of a compatible system. Check the test configuration, required chamber condition and prescribed position. Run the specified test programme rather than substituting a routine load cycle. At the instructed stage, retrieve and assess the indicator without changing the test assembly beforehand.

Reading and documenting the result

Assess uniformity across the entire indicator pattern using its own reference. An unexpected pattern requires investigation of the test setup and sterilizer performance. Record the cycle identifier, date, operator and result. Do not interpret a changed external package mark as the internal Bowie-Dick test result.

Practical benefits

A defined test format gives the team a consistent observation to record and discuss with technical staff. Keeping the actual result helps subsequent troubleshooting. Passing the test does not release later instrument loads and does not replace their required monitoring.

Selection questions

Confirm the sterilizer model, approved test programme and required test system before ordering. A card and a complete pack are not automatically interchangeable. Do not infer a diagnosis of a specific mechanical fault solely from one colour pattern; investigate the result using the relevant procedure.

Questions before ordering

What should I include in a technical enquiry?

Include the exact product name or code, equipment, process, packaging material and intended monitoring task. If you are replacing an existing product, provide its instructions and explain the application rather than requesting equivalence by appearance alone. Krinmed can then identify the relevant model documentation for your evaluation.

Can I use an image as the result reference?

No. Screen colour, lighting and image processing can alter the appearance of an indicator. Read an actual test against the current reference and instructions supplied for that product. Website photographs support identification and presentation; they are not a calibrated colour standard.

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