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CP-Pumpen - Model MKP-Bio -Stainless Steel Magnetic Drive Biotech Process Pump
FromCP Pumpen AG
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
