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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
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Introducción del producto

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.

Características clave

Glove positions are spaced for simultaneous sample opening and test manipulation.

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.

Soluciones para su aplicación

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.

Aplicaciones típicas

Sterile drug sterility testingMedical-device sterility testingMembrane filtration methodsDirect inoculation procedures

Parámetros técnicos

Typical configurable construction ranges for a sterility test isolator are listed below.

Materiales CoreFully welded SUS316L test chamber with laminated safety glass and CSM glove-sleeve assemblies
Panel de espesorCámara de doble piel de 50-100mm y secciones de tratamiento de aire
Ancho efectivo1800-4500 mm usable test-chamber width
Longitud máximaUp to 6500 mm overall isolator length
Acero frente a espesorCarcasa de cámara SUS316L de 2,0 a 3,0mm; fundas de servicio de 1,2 a 1,5mm
Densidad CoreAproximadamente 8000 kg/m³ para el material de la Cámara SUS316L
Conductividad térmica14-16 W/(m · K) para acero inoxidable austenítico
Superficie acabadaElectropolished SUS316L test chamber with welded radiused transitions
Tipo conjuntoPressure-tight welded chamber with sealed glove rings, transfer hatch and separate waste interfaces
CustomizationDisponible según la aplicación prevista y el entorno operativo.

Opciones disponibles

Single- or dual-operator chamberBio-descontaminación integrada de vaporPuertos de transferencia rápidaMembrane filtration and waste handling modules

Planning a Sterility Test Isolator specification?

Envíenos sus dimensiones, condiciones de instalación, objetivos de rendimiento y acabado superficial requerido.

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