Sartorius® Sartopore 2 MidiCaps,0,1µm,BH9,4pcs, Sartopore 2 MidiCaps

Sartopore® 2 0.1 µm MidiCaps are ready-to-use, individually packaged membrane filter elements for valid sterile filtration and reliable removal of Mycoplasma in the pharmaceutical/biotech industry. Applications: Typical applications include sterile filtration and mycoplasma removal of: - Animal sera - Cell culture media - Media components - Bioprocess pharmaceuticals - Biological solutions. Any other application requires less than 0.2 µm filtration for increased sterility assurance. Compatibility: The polyethersulfone membrane is compatible within a pH range of 1-14, making Sartopore 2 MidiCaps ideal for filtration of high/low pH solutions. Easy handling: Sartopore® 2 capsules are supplied as individually packaged sterile elements. This partially eliminates the need for sterilization prior to use. Flexibility: Sartopore® 2 0.1 µm MidiCaps are available with different filtration areas from 0.6m² | 6 ft² to 1.8 m² |18 ft². This allows you to easily use them in any filtration process regardless of batch size. Scalability: Consistent and predictable scale-up and scale-down processes can be reliably performed as all Sartopore® 2 MidiCaps are produced with the same membrane type and identical construction materials. Cost savings: By using single-use capsules, investments in stainless steel filter housings are avoided and additional costs for cleaning the housings and their validation are saved. Microbiological retention: Sartopore® 2 0.1 µm MidiCaps have been validated with a Log Reduction Value (LRV) of 7 for "Acholeplasma laidlawii" according to ASTM F-838-05 specifications. Quality control: Each individual element was tested for integrity by a diffusion test prior to release to ensure absolute reliability. Documentation: Sartopore® 2 MidiCaps were designed, developed and manufactured in accordance with an ISO 9001 certified quality management system. A validation and extractable manual, in accordance with regulatory requirements, is available. Single-Use MidiCaps® for Process Scale Reduction of Cleaning & Cleaning Validation Familiar performance characteristics of Sartopore® 2 applications: Typical applications include sterile filtration and mycroplasma removal of: - Animal serum - Cell culture media - Media components - Bioprocess pharmaceuticals - Biological solutions. Any other application requires less than 0.2 µm filtration for increased sterility assurance. Typical applications include sterile filtration and mycroplasma removal of: Animal serum Cell culture media Media components Bioprocess pharmaceuticals Biological fluids Any other application requiring less than 0.2 µm filtration for increased sterility assurance Compatibility: The polyethersulfone membrane is compatible within a pH range of 1-14, making Sartopore® 2 MidiCaps ideal for filtration of high/low pH solutions. Easy handling: Sartopore® 2 capsules are supplied as individually packaged sterile elements. This partially eliminates the need for sterilization prior to use. Flexibility: Sartopore® 2 0.1 µm MidiCaps® are available with different filtration areas from 0.6m² | 6 ft² to 1.8 m² |18 ft². This allows you to easily use them in any filtration process regardless of batch size. Scale Up: Consistent and predictable scale-up and scale-down processes can be performed with operational confidence because all Sartopore® 2 MidiCaps® are manufactured with the same membrane type and identical materials of construction. Cost savings: By using single-use capsules, investments in stainless steel filter housings are avoided and additional costs for cleaning the housings and their validation are saved. Microbiological retention: Sartopore® 2 0.1 µm MidiCaps® have been validated with a Log Reduction Value (LRV) of 7 for "Acholeplasma laidlawii" according to ASTM F-838-05 specifications. Quality Control: Each individual element was tested for integrity by diffusion testing prior to release to ensure absolute reliability. Documentation: Sartopore® 2 MidiCaps® were designed, developed and manufactured in accordance with an ISO 9001 certified quality management system. A validation and extractable manual, in accordance with regulatory requirements, is available.