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CP-PumpenModel MKP-Bio -Stainless Steel Magnetic Drive Biotech Process Pump

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Discover the benefits of the MKP Bio produced by CP here - the CIP pump for sterile processes in the pharmaceutical and biotech industry.

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Special features

  • 100 % drainable (no flushing, drain or ventilation connections
  • 100 % cleanable (CIP)
  • 100 % sterilisable (SIP)
  • self-venting
  • parts in contact with medium: Surface quality Ra ≤ 0.8, inside edges R3, surfaces inclined > 3°

Construction

  • compact & free of dead space
  • no shaft feedthrough & leak-free
  • single-part & central bearing
  • vertical installationno shaft seal (=no penetration by micro-organisms)
  • no plain bearing carrier
  • single-part, centrally arranged impeller bearing with optimal cooling and flushing (=optimal running properties)
  • low bearing forces due to hydraulically balanced impeller
  • high material flexibility
  • inverted drive principle

Assembly & repair

  • modular system made up of few individual parts
  • assembly friendly
  • impeller can be removed without tools

Standard

  • DIN EN ISO 5199, 15783
  • DIN EN 12462

Directives

  • CIP
  • SIP
  • EHEDG
  • EC Machinery Directive
  • EC ATEX Directive
  • FDA + EU 1935/2004
  • Hygiene standards 3A

Capacities 

  • 0.5 to 60 m3/h

Heads

  • 5 to 80 m

Pressure rating

  • PN 16

Temperatures

  • -20 to +150°C

Kinematic viscosities 

  • 0.5 to 350 mm2/s

Solid handlings 

  • gut geeignet

Casing materials

  • Stainless steel 1.4404/1.4435 (316L)
  • Other materials
  • Stainless steel (e.g. 1.4306, Uranus® B6), duplex alloys (e.g. 1.4517), nickel-base alloys (e.g. Hastelloy® C-4, C-22)

Working Principle

  • Radial flow pump

Stage 

  • Single stage

Priming Method 

  • Flooded suction

Sealing System 

  • Magnetic coupling

Configurations

  • CP`s standard configuration: Close-coupled (-20°C to +150°C)
  • Mounting arrangement: Vertical

EC Directives  

  • 2006/42/EG (Machinery), 2014/34/EU (ATEX)

Standards  

  • DIN EN 12462 / DIN EN ISO 5199,15783

Other Regulations 

  • Hygienestandards 3-A, EHEDG, VDMA, FDA 21 CFR §177