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Isolador de teste de esterilidade

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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Introdução do produto

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-chave

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.

Preocupações do produto do cliente

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.

Aplicações típicas

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

Parâmetros técnicos

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

Material principalFully welded SUS316L test chamber with laminated safety glass and CSM glove-sleeve assemblies
Painel de espessura50-100 mm double-skin chamber and air-handling sections
Largura efetiva1800-4500 mm usable test-chamber width
Comprimento máximoUp to 6500 mm overall isolator length
Aço enfrentando espessura2.0-3.0 mm SUS316L chamber shell; 1.2-1.5 mm service skins
Densidade CoreApproximately 8000 kg/m³ for SUS316L chamber material
Condutividade térmica14-16 W/(m·K) for austenitic stainless steel
Superfície acabadoElectropolished SUS316L test chamber with welded radiused transitions
Tipo conjuntoPressure-tight welded chamber with sealed glove rings, transfer hatch and separate waste interfaces
CustomizaçãoDisponível com base na aplicação pretendida e no ambiente operacional.

Opções disponíveis

Single- or dual-operator chamberIntegrated vapor bio-decontaminationRapid transfer portsMembrane filtration and waste handling modules

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