Mar Cor Purification Pharmaceutical Reverse Osmosis System H2Pro

Description
20 to 450 USGPM The H2Pro model of reverse osmosis system sis Mar Cor Purification’s highest quality water treatment system. These systems are designed to produce pharmaceutical grade product water from any potable source and be fully heat sanitizable to ensure sanitary operating conditions. System Suitability TOC monitoring can be done on-line or in the lab with a TOC analyzer of better then 50 ppb detection. All analyzers must be periodically challenged with a system suitability solution of 500 ppb USP 1.4 benzoquinone RS. In both cases the analyzers efficiency must be no lower then 85% and not higher then 115%. USP 27 Conductivity Method Compliance System verification is allowed within the USP specified 0.1 uS/cm, using a special NIST traceable resistor that plugs into an end-panel receptacle. Similarly, a pre-packaged, NIST traceable calibration standard confirms / calibrates the cell constant to within the specified 2%. Conductivity is reported as non-temperature compensated, and alarm outputs are based on the Stage 1 parameters established in the USP conductivity method.
Datasheet
Description
20 to 450 USGPM The H2Pro model of reverse osmosis system sis Mar Cor Purification’s highest quality water treatment system. These systems are designed to produce pharmaceutical grade product water from any potable source and be fully heat sanitizable to ensure sanitary operating conditions. System Suitability TOC monitoring can be done on-line or in the lab with a TOC analyzer of better then 50 ppb detection. All analyzers must be periodically challenged with a system suitability solution of 500 ppb USP 1.4 benzoquinone RS. In both cases the analyzers efficiency must be no lower then 85% and not higher then 115%. USP 27 Conductivity Method Compliance System verification is allowed within the USP specified 0.1 uS/cm, using a special NIST traceable resistor that plugs into an end-panel receptacle. Similarly, a pre-packaged, NIST traceable calibration standard confirms / calibrates the cell constant to within the specified 2%. Conductivity is reported as non-temperature compensated, and alarm outputs are based on the Stage 1 parameters established in the USP conductivity method.
Datasheet

Suppliers

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Product
Description
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Pharmaceutical Reverse Osmosis System - H2Pro - Mar Cor Purification
Skippack, PA, USA
Pharmaceutical Reverse Osmosis System
H2Pro
Pharmaceutical Reverse Osmosis System H2Pro
20 to 450 USGPM The H2Pro model of reverse osmosis system sis Mar Cor Purification’s highest quality water treatment system. These systems are designed to produce pharmaceutical grade product water from any potable source and be fully heat sanitizable to ensure sanitary operating conditions. System Suitability TOC monitoring can be done on-line or in the lab with a TOC analyzer of better then 50 ppb detection. All analyzers must be periodically challenged with a system suitability solution of 500 ppb USP 1.4 benzoquinone RS. In both cases the analyzers efficiency must be no lower then 85% and not higher then 115%. USP 27 Conductivity Method Compliance System verification is allowed within the USP specified 0.1 uS/cm, using a special NIST traceable resistor that plugs into an end-panel receptacle. Similarly, a pre-packaged, NIST traceable calibration standard confirms / calibrates the cell constant to within the specified 2%. Conductivity is reported as non-temperature compensated, and alarm outputs are based on the Stage 1 parameters established in the USP conductivity method.

20 to 450 USGPM

The H2Pro model of reverse osmosis system sis Mar Cor Purification’s highest quality water treatment system. These systems are designed to produce pharmaceutical grade product water from any potable source and be fully heat sanitizable to ensure sanitary operating conditions.

System Suitability

TOC monitoring can be done on-line or in the lab with a TOC analyzer of better then 50 ppb detection. All analyzers must be periodically challenged with a system suitability solution of 500 ppb USP 1.4 benzoquinone RS. In both cases the analyzers efficiency must be no lower then 85% and not higher then 115%.

USP 27 Conductivity Method Compliance

System verification is allowed within the USP specified 0.1 uS/cm, using a special NIST traceable resistor that plugs into an end-panel receptacle. Similarly, a pre-packaged, NIST traceable calibration standard confirms / calibrates the cell constant to within the specified 2%. Conductivity is reported as non-temperature compensated, and alarm outputs are based on the Stage 1 parameters established in the USP conductivity method.

Supplier's Site Datasheet

Technical Specifications

  Mar Cor Purification
Product Category Filtration Equipment
Product Number H2Pro
Product Name Pharmaceutical Reverse Osmosis System
Equipment Type Reverse Osmosis
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