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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.
All gasket materials comply with the FDA regulations 21 CFR 17.2600 and USP Class VI
Connections (Physical)
Closure System
Tri clamp connection acc. to DIN 32676 with clamp
Connector(s)
Sanitary tri-clamp similar acc. to DIN 32676 DIN DN 10 TC 50.5 mm
General Specifications
Surface Finish
Ra < 0.5 µm internal (Electropolished sufaces), Ra < 1.6 µm external (Electropolished sufaces)
Materials of Construction
Housing Material
AISI 316L (1.4404) stainless steel
AISI 316L (1.4435) stainless steel
Sealing Material
Silicone (SI)
Seals
Silicone (FDA, Code 21 CFR 17.2600 / USPcIVI)
Operating Conditions
Maximum Allowable Working Temperature
150 °C (302 °F)
Maximum Operating Pressure
4 bar (58 psi)
Product Information
Qualification Documents
With standard documentation
Type
Pressure Vessel
Volume
Volume
30 L
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