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InnoScreen COVID 19 Antigen Rapid Testing Kits

Box of 20 test kits

In stock
SKU
SCOV-23

The InnoScreen™ COVID-19 Antigen Rapid Test Kit is approved by the TGA for Supply in Australia

As the disease (‘COVID-19”) has achieved pandemic status. There is an upsurge of infective coronavirus (SARS-CoV-2) and has generated significant global concern. While laboratory testing of nasopharyngeal swabs for active virus load represents the gold standard of infection testing and tracing, implementing on-site rapid testing for COVID-19 allows businesses to maintain a COVID-safe workplace. DJO has partnered with Innovation Scientific and is now offering InnoScreen COVID-19 Antigen Rapid Test kits for sale to business clients.

Why should we conduct on-site rapid testing?

As businesses return to a sense of normality, business need to take appropriate actions to maintain workplace safety. On-site screening may provide an immediate indication as to the possible infectivity of any individual on a given worksite.

INNOSCREEN™ COVID-19 Antigen Rapid Test Kit, Is It Approved by the TGA ?

Yes, it is. Find the InnoScreen COVID-19 Antigen Rapid Test Device listed on the TGA site here.

What is included in the Box of each kit?

The equipment required to perform 20 individual tests contains in each kit:

  • Individually packed test device - 20
  • Extraction tube with buffer - 20
  • Sample collection swab - 20
  • Tube stand - 1
  • Instruction Guide - 1

Who should conduct the INNOSCREEN™ Antigen Rapid Test’s?

Tests must be conducted or supervised by a health practitioner as defined in Section 3 of the Therapeutic Goods Act 1989. Additionally, they must undergo education provided on the DJOstore on correct use of the device and interpretation of the test result.

Education?

Yes. There is a video and a procedure card to support from our trained health practitioners.

Who can purchase the test?

DJO is able to sell to government, health practitioners and companies who employs or occupies a health practitioner as defined in Section 3 of the Therapeutic Goods Act 1989 who is responsible for performing or supervising the performance of the test and undertakes suitable education on the testing device. The federal and state government in counsel with the TGA will up new regulations from early November.

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Healing and wellness through the benefit of natural motion have always been at the center of our story.

Our company philosophy - ‘To get and keep people moving,’ is based on the idea that activity is the key to healthier lives, better outcomes and improved healthcare economics for all.

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