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      Protein Residue Test Kit

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      —Protein Residue Test Kit
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      protein residue test
      rapid protein residue test
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      protein swab test
      Protein residue test kit for surgical instruments and endoscope cleaning verification
      protein residue test
      protein residue test
      rapid protein residue test
      protein residue clean test
      rapid protein residue test
      cleaning verification test
      protein swab test
      Protein residue test kit for surgical instruments and endoscope cleaning verification
      protein residue test
      In stock
      SKU 5646854
      MEDIWISH

      A protein residue test for checking sampled surfaces after cleaning. Product reference 5646854. The existing catalogue states a 10-second visual response; confirm the current product IFU for sampling, readout and acceptance criteria.

      Details
      Characteristics
      Process
      —
      Cleaning
      Analyte
      —
      Protein
      Type
      —
      Protein Residue Test
      Test Type
      —
      Protein Residue Test
      Monitoring Purpose
      —
      Residual Protein Detection
      Applicable Equipment
      —
      Ultrasonic Cleaner, Washer-Disinfector
      All characteristics
      Protein Residue Test
      This is an indicative end-user reference price for budgetary guidance only and does not constitute a formal quotation.
      Please include in your request: product name or model, dimensions and specifications, quantity and destination country. For OEM or private-label projects, add your packaging and labeling requirements.
      • Description
      • Characteristics
      • Ordering & Delivery

      Check residual protein after cleaning

      The MEDIWISH Protein Residue Test, reference 5646854, is intended for residual-protein checks on sampled surfaces after cleaning. It addresses residue remaining at the sampled location, a different question from cavitation activity in an ultrasonic bath.

      A result applies to the sample and conditions of the method. It does not establish that the entire instrument is free of all contamination, disinfected or sterile, and it does not replace the facility's complete cleaning verification and release procedure.

      Product parameters and current instructions

      The existing catalogue for this reference states a sensitivity of 0.1 μg, a 10-second visual response and a colour change from light brown to blue. It describes surface sampling with a swab followed by contact with the reagent. These stated values are retained; they must not be transferred from or to another protein test.

      Request the current IFU for reference 5646854 before use. A product-specific IFU is not currently linked on this page. Confirm the supported sample type, sampling area and recovery, reagent handling, temperature, reading window, detection-limit conditions and acceptance criteria. The catalogue's 0.1 μg figure is not by itself a universal acceptance threshold or a value per unit area. Do not introduce heating, incubation or a different sampling method without the applicable IFU.

      Interpret and record within the method

      Use the current instructions to distinguish valid, positive, negative and invalid outcomes. Record the product reference and lot, expiry, sampled item and location, test conditions, reading time and result. A result indicating residue calls for review under the facility procedure; a negative result does not prove absence of all protein outside the method's detection and recovery limits.

      How this differs from an ultrasonic indicator

      MZS-5635 cavitation indicator vials assess a qualitative response at a defined bath location. They do not sample protein from an instrument. A protein residue test and a cavitation check can answer separate monitoring questions; neither substitutes for the other.

      Use the comparison of cleaning monitoring methods to distinguish their purposes, or return to cleaning validation and monitoring products.

      Questions before ordering

      Is this an ATP or sterility test?

      No. This listing concerns residual protein. It does not establish ATP content, microbial kill or sterility.

      Can one result represent every instrument surface?

      No. Interpretation depends on the sampled location and the validated sampling and test conditions. Confirm suitability for the intended instrument, surface or channel in the current instructions.

      Which documents and pack details should I request?

      Ask for the current IFU and specification for reference 5646854, the supplied components, quantity per pack, storage and shelf life, and documentation required for your intended market. Do not assume the specification of another MEDIWISH protein test applies.

      Request product documentation and a quotation. Include reference 5646854, intended sample, instrument or surface, destination country and required quantity.

      Process
      ?
      Types of sterilization, control of the intended sterilization method
      Cleaning
      Analyte
      Protein
      Type
      Protein Residue Test
      Test Type
      Protein Residue Test
      Monitoring Purpose
      Residual Protein Detection
      Applicable Equipment
      Ultrasonic Cleaner, Washer-Disinfector
      Advantages
      Clear colour change; sensitive detection of residual protein
      Features
      Rapid visual result in approximately 10 seconds; no incubation required
      Usage
      Cleaning verification for residual protein after manual cleaning, ultrasonic cleaning and washer-disinfector processing of surgical instruments, endoscope channels and hard-to-clean surfaces.
      USE
      Rapid visual test to detect protein residues on instruments and surfaces after cleaning.
      Indicator Color Change
      Light brown to blue
      Quantity in box
      25 tests / box
      Packaging Details
      25 test vials + 25 swabs
      Quality Certification
      EN ISO 15883
      Indicator Change
      Light brown → blue
      Packaging
      25 test vials + 25 swabs, 25 tests / box

      Send your request with the product name or model, required specifications, quantity and destination country. Product configuration and payment and delivery terms are agreed when the order is confirmed.

      Ordering, payment and delivery information

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