NO CROSS CONTAMINATION
All SteriWare® devices are supplied ready to use straight from the bag and are designed for single use.
This prevents cross-contamination from previous samples, cleaning agents or environmental contaminants and ensures that foreign substances do not interfere with sampling and testing.
NO CLEANING REQUIRED
Unlike reusable devices, disposable SteriWare® products do not require cleaning after use.
Cleaning reusable sampling equipment can be expensive, time-consuming and difficult, especially when handling oily, adhesive or hazardous substances.
Using disposable equipment removes cleaning costs, eliminates cleaning validation requirements and saves valuable operator time.
THE HIGHEST QUALITY
Each SteriWare® device is manufactured and packed within a Class 100,000 cleanroom facility in the United Kingdom.
Every product undergoes inspection prior to packing to maintain the exceptional quality standards for which Sampling Systems is known.
Detailed manufacturing information can be found in the relevant Certificates of Conformity and Technical Specification Sheets.
FULL DOCUMENTATION
Comprehensive batch-specific documentation is available across the entire SteriWare® product range.
- Batch numbers printed on every bag and box.
- Certificates of Conformity available.
- Certificates of Irradiation supplied where applicable.
- Full traceability documentation.
- Technical Specification Sheets available for download.
A CLASS-LEADING RANGE
Sampling Systems pioneered the introduction of cleanroom-manufactured disposable samplers and continues to offer one of the world's largest ranges of single-use sampling equipment.
Our extensive portfolio includes solutions for:
- Powders and granules
- Liquids and viscous materials
- Single-point sampling
- Multi-level sampling
- Cross-sectional sampling
- Sterile and aseptic applications
AVAILABLE STERILE
Most SteriWare® products are available pre-sterilised to SAL 10⁻⁶ standards.
Please refer to the individual product specification sheet for full details regarding sterilisation validation and documentation.