CADY COVID-19 Antigen Rapid Test

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The CADY COVID-19 Antigen Rapid Test is a colloidal gold antigen rapid test kit for in vitro qualitative detection of SARS-COV-2. Intended for use by clinical laboratories or healthcare workers for point-of-care testing, not for at-home testing.
● Minimum Order Quantity: 200 kits
● Seller Name: ReVital
● Seller Location: Kenya
● Warranty Term: Not applicable
● Regulatory Approvals: CE; ISO 13485; Kenyan Pharmacy and Poisons Board

Additional information

Weight 3.50 kg
Dimensions 42.50 × 34.00 × 22.00 cm

Description

The CADY COVID-19 Antigen Rapid Test is a colloidal gold antigen rapid test kit for in vitro qualitative detection of SARS-CoV-2 nucleocapsid antigen in nasal (NS) swab specimens directly from individuals who meet COVID-19 clinical and / or epidemiological criteria. CADY COVID-19 Antigen Rapid Test Kit is for professional use only and is intended to be used as an aid in the diagnosis of SARS-CoV-2 infection. The product may be used in any laboratory and non-laboratory environment that meets the requirements specified in the Instructions for Use and local regulation.
Read our Buyer's Guides to learn more about Covid-19 Testing.

Key Features

Usability
This test provides less invasive sample collection with nasal swabs. No instrumentation required. This is a cost-effective solution for large-scale testing.

Reliable Rapid Detection
The CADY COVID-19 Antigen Rapid Test was tested by an independent clinical study in Europe and shown high performance. It offers rapid detection of SARS-CoV-2 nucleocapsid antigen in less than 15 minutes.

Specifications

Performance

  • Sensitivity: 98.72% (100% for samples with Ct values ≤33)
  • Specificity: 97.32%
  • Test Time: 15–20 minutes
  • Storage Condition : 2°C–30°C
  • Sample Type: Nasal (Ns) swab
  • Shelf Life: 24 months

Standard Accessories

Each test includes:

  • Buffer bottle (350 μL/bottle) (1x)
  • Sterilized nasal (NS) swab (1x)
  • Extraction tube and nozzle cap (1x)

Optional Accessories & Add-ons

Not applicable

Product Documents, Manuals & Brochures

Brochure

Insert

Specifications

Regulatory Certificates

ISO 13485

Kenya PPB

Declaration of Conformity

Videos

Not available at this time

 

FAQ

Not available at this time

 

Studies & Trials

  • Clinical Study Population: 190 Individuals, Including 78 PCR-Positives And 112 PCR-Negatives
  • Clinical Study Date & Location: November 2020 Apollosa (Benevento) Italy

Package Contents

  • 20x Test Kits
  • 20x Buffer bottles (350 μL/bottle)
  • 20x Sterilized nasal (NS) swabs
  • 20x Extraction tubes and nozzle caps
  • 1x Instructions

Warranty

Not applicable
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