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Équipement d'écoulement et de confinement laminaires
Test de stérilité isolateur
A closed glove-access isolator arranged for sterility testing workflows, controlled sample entry and separate removal of liquid and solid waste.
- Dedicated Sterility Test Layout
- Dual-Operator Glove Access
- Controlled Sample Transfer
- Separated Waste Removal
Introduction de produit
The sterility test isolator separates test samples and media from operators and the surrounding laboratory. One or two glove-access work chambers can support membrane filtration, direct inoculation or compatible rapid methods. Samples enter through a bio-decontamination hatch or rapid transfer port, and liquid and solid waste leave through dedicated closed routes. The chamber uses filtered airflow, welded stainless surfaces and pressure monitoring to maintain the selected test environment and reduce false-positive contamination risk.
Key Features
A dedicated transfer hatch separates load preparation from the main test chamber.
Separate liquid and solid waste interfaces prevent waste crossing the clean sample route.
A common control system monitors pressure, airflow and optional bio-decontamination cycles.
Radiused stainless interiors keep membrane-filtration equipment accessible for cleaning.
Préoccupations du client produit
Sterility testing needs both contamination prevention and a workflow that keeps sample entry, test manipulation and waste removal from crossing each other.
Room-borne contamination creates false-positive test results.A closed filtered chamber and controlled transfer path isolate the test from the laboratory.
Two operators cannot reach the same test setup efficiently.Paired glove positions and a long work zone support parallel manipulation.
Waste removal crosses the incoming sample path.Dedicated liquid and solid waste ports separate egress from sample loading.
Test equipment creates inaccessible surfaces.Removable supports and radiused internal geometry preserve cleaning access.
Les applications typiques
Sterile drug sterility testingMedical-device sterility testingMembrane filtration methodsDirect inoculation procedures
Paramètres techniques
Typical configurable construction ranges for a sterility test isolator are listed below.
| Matériaux de base | Fully welded SUS316L test chamber with laminated safety glass and CSM glove-sleeve assemblies |
|---|---|
| Panneau épaisseur | 50-100 mm double-skin chamber and air-handling sections |
| Largeur effective | 1800-4500 mm usable test-chamber width |
| Longueur maximale | Up to 6500 mm overall isolator length |
| Acier face épaisseur | 2.0-3.0 mm SUS316L chamber shell; 1.2-1.5 mm service skins |
| Densité Core | Approximately 8000 kg/m³ for SUS316L chamber material |
| Conductivité thermique | 14 - 16 W / (m · K) pour l'acier inoxydable austénitique par |
| surface finie | Electropolished SUS316L test chamber with welded radiused transitions |
| Type joint | Pressure-tight welded chamber with sealed glove rings, transfer hatch and separate waste interfaces |
| Customisation | Disponible en fonction de l'application prévue et de l'environnement d'exploitation. |
Options disponibles
Single- or dual-operator chamberIntegrated vapor bio-decontaminationRapid transfer portsMembrane filtration and waste handling modules
Planning a Sterility Test Isolator specification?
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