Exotic Pets | Reptile Colloidal Gold Rapid Test
Reptile Salmonella / Cryptosporidium Ag Combo Rapid Test Kit
For qualitative combined detection of Salmonella and Cryptosporidium antigens in reptile feces or cloacal swab specimens to support rapid gastrointestinal pathogen screening.
Overview
Product Features
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
| Intended use | For qualitative combined detection of Salmonella and Cryptosporidium antigens in reptile feces or cloacal swab specimens to support rapid gastrointestinal pathogen screening. |
|---|---|
| Method | Colloidal gold immunochromatography |
| Format | Rapid test cassette |
| Target analyte | Salmonella and Cryptosporidium antigens |
| Species | Reptiles covered by the IFU |
| Specimen | Feces / cloacal swab |
| Result time | 10 minutes |
| Storage | 2-30°C |
| Pack size | 10 Tests/Kit |
| Main components | Individually pouched cassette, sample extraction tube, disposable swab/sampling accessories and IFU |
| Use | Professional veterinary in vitro diagnostic use |
Testing Workflow
- 1 Collect fresh feces or a cloacal swab specimen and mix it with sample buffer as instructed in the IFU.
- 2 Apply the specified volume or drops of processed specimen to the cassette sample well.
- 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.