Exotic Pets | Reptile Colloidal Gold Rapid Test

Reptile Cryptosporidium Ag Rapid Test Kit

For qualitative detection of Cryptosporidium antigen in reptile feces or cloacal swab specimens to support rapid gastrointestinal parasite screening.

10 Tests/Kit 10 minutes 2-30°C Colloidal gold immunochromatography
Reptile Cryptosporidium Ag Rapid Test Kit

Overview

Caracteristicas del producto

Rapid screening for reptile gastrointestinal targets

Built for veterinary, laboratory and field screening workflows in turtles, lizards, snakes and other IFU-covered reptiles.

Feces / cloacal swab workflow

Matches practical reptile sampling needs for clinic and husbandry-management scenarios.

Visual C/T line reading

The colloidal gold lateral-flow format can be interpreted within the defined reading window.

10 Tests/Kit channel-ready packaging

Aligned with Safheal companion-animal rapid test packaging for stocking and distribution.

Professional Kit Configuration

Individually pouched cassette, sample extraction tube, disposable swab/sampling accessories and IFU.

Specifications

Uso previsto For qualitative detection of Cryptosporidium antigen in reptile feces or cloacal swab specimens to support rapid gastrointestinal parasite screening.
Metodo Colloidal gold immunochromatography
Formato Rapid test cassette
Objetivo analyte Cryptosporidium antigen
Species Reptiles covered by the IFU
Muestra Feces / cloacal swab
Result time 10 minutes
Almacenamiento 2-30°C
Tamano del kit 10 Tests/Kit
Componentes principales Individually pouched cassette, sample extraction tube, disposable swab/sampling accessories and IFU
Use Professional veterinary in vitro diagnostic use

Testing Flujo de trabajo

  1. 1 Collect fresh feces or a cloacal swab specimen and mix it with sample buffer as instructed in the IFU.
  2. 2 Apply the specified volume or drops of processed specimen to the cassette sample well.
  3. 3 Read the C/T line result within the defined interpretation window; do not interpret expired reads.

Note

This page is a product overview. Final specimen volume, procedure, registered intended use and performance data should follow the package insert and local regulatory requirements.