Biopharma Pressure Vessel Type 380 | 10 L
Choose your Pressure Vessels
Our pressure vessels are manufactured in facilities certified for compliance with the European Pressure Equipment Directive 2014/68/EU. Flexibility, thorough cleanability and ease of use are the major features of our pressure vessels. Sartorius Stedim Biotech pressure vessels are designed to fulfill our customers’ quality standards and thus completely meet market expectations.
Compliance Information
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CFR ComplianceAll gasket materials comply with the FDA regulations 21 CFR 17.2600 and USP Class VI
Connections (Physical)
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Closure SystemTri clamp connection acc. to DIN 32676 with clamp
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Connector(s)Sanitary tri-clamp similar acc. to DIN 32676 DIN DN 10 TC 50.5 mm
General Specifications
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Surface FinishRa < 0.5 µm internal (Electropolished sufaces), Ra < 1.6 µm external (Electropolished sufaces)
Materials of Construction
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Sealing MaterialSilicone (SI)
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SealsSilicone (FDA, Code 21 CFR 17.2600 / USPcIVI)
Operating Conditions
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Maximum Allowable Working Temperature150 °C (302 °F)
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Maximum Operating Pressure4 bar (58 psi)
Product Information
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Qualification DocumentsWith standard documentation
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TypePressure Vessel
Volume
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Volume10 L