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A compact aseptic laboratory isolator that controls sterility testing through HEPA airflow, automated H2O2 decontamination and integrated membrane-filtration workstations.
- Controlled Test Environment
- Integrated Filtration Pumps
- Rapid H2O2 Cycle
- Monitored Test Workflow
Introducción del producto
The sterility test isolator provides closed work chambers for membrane-filtration or direct-inoculation testing. Stainless construction, HEPA-controlled airflow and fixed glove access protect the test from room contamination, while a dedicated transfer airlock and automated hydrogen-peroxide cycle prepare incoming materials and internal surfaces. Integrated pumps, bottle racks and process monitoring support repeatable laboratory campaigns with fewer handling steps.
Características clave
Integrated membrane-filtration pumps reduce loose equipment and tubing inside the chamber.
Automated H2O2 decontamination treats both work chamber and material airlock.
Continuous pressure, cycle and environmental monitoring supports documented operation.
Soluciones para su aplicación
Sterility testing is vulnerable to false positives from environmental ingress and false negatives if decontamination residues are not adequately aerated.
Room-borne organisms can contaminate exposed test assemblies.A sealed HEPA-controlled barrier isolates samples and media from the laboratory background.
Complex material entry increases contamination risk and test delay.A dedicated airlock decontaminates organized loads before chamber transfer.
Loose pumps and tubing create clutter and cleaning difficulty.Integrated filtration pumps and fixed racks simplify setup and surface access.
Inconsistent cycle records weaken investigation traceability.Automated controls record pressure, decontamination and aeration parameters for each run.
Aplicaciones típicas
Pharmaceutical batch-release sterility testingMembrane-filtration microbiology testsDirect-inoculation sterility testsAseptic quality-control sample handling
Parámetros técnicos
Typical construction values for a modular pharmaceutical sterility test isolator are listed below.
| Materiales Core | 316L stainless steel chambers with safety-glass windows and CSM or EPDM glove sleeves |
|---|---|
| Panel de espesor | 40-80 mm double-skin enclosure panels |
| Ancho efectivo | 1200-2800 mm test chamber width |
| Longitud máxima | Up to 4500 mm modular isolator length |
| Acero frente a espesor | 1,2-1,5mm pieles de acero inoxidable |
| Densidad Core | 80-140 kg/m³ para relleno de panel sellado |
| Conductividad térmica | 0.038-0.055 W/(m · K) para relleno de panel aislado |
| Superficie acabada | Satin 316L stainless steel with radiused, cleanable internal surfaces |
| Tipo conjunto | Continuously welded chambers with gasketed windows, clamped HEPA housings and sealed transfer-airlock interface |
| Customization | Disponible según la aplicación prevista y el entorno operativo. |
Opciones disponibles
Membrane-filtration or direct-inoculation workstationPositive or negative pressure operationIntegrated particle counter and air samplerWireless glove testing and data reporting
Planning a Sterility Test Isolator specification?
Envíenos sus dimensiones, condiciones de instalación, objetivos de rendimiento y acabado superficial requerido.
