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E-mail
bestestbio@126.com
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Phone
18621924707,15221692185
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Address
No. 13, Lane 506, Sanlin Town, Pudong New Area, Shanghai
Shanghai Bitai Biotechnology Co., Ltd
bestestbio@126.com
18621924707,15221692185
No. 13, Lane 506, Sanlin Town, Pudong New Area, Shanghai
Sartorius Midisart 2000 PTFE gas filter
Midisart®The 2000 filter is an ideal tool for use in biotechnology, pharmaceutical industries, research institutes, and any place that requires sterile ventilation, biological isolation, or sterile air and gas.
Midisart®2000 has * sterile ventilation function in filling containers and fermentation bottles, including culture containers and CO2Incubator (6-120L)
-Aseptic ventilation of sterile, distilled water, and liquid medium culture tanks
-High pressure sterilization ventilation
-Online sterilization and removal of air and gas particles, such as sterile ventilation in small fermentation tanks.
Midisart®The 2000 filter achieves optimal operation for simple and safe handling. The conical hose hook ensures simple and safe use of hoses with an inner diameter of 6-12mm. Midisart®2000 is lightweight - only 20-g - so it won't bend the hose and hinder the ventilation function.
User benefits:
1. Optimal operation: - Midisart®2000 individually packaged, pre disinfected, ready to use connection!
2. Reliability and safety: Midisart®2000 has complete testability and provides reproducible results.
The filter membrane adopts polypropylene mesh reinforcement technology, with a pressure resistance of up to 3 bar (about 44 psi).
Midisart®2000 can eliminate moisture by using a hydrophobic PTFE membrane. Apart from this Midisart®Due to all its materials passing USP Plastic VI standard testing, 2000 has biological safety.
Midisart®2000 can withstand at least 20 high-pressure sterilization cycles without damaging its performance. Each Midisart®2000 provides convenient storage disks with UPN codes to ensure that you can track each high-pressure sterilization. This critical feature meets the requirements of GLP and ISO for traceability documents.
3. Quality Control Certificate:
-The casing of each component undergoes automatic integrity testing, and the sealing of the membrane during manufacturing is part of the product quality control testing.
To ensure product quality, the production batch number and product serial number are printed on the outer shell of each filter. Midisart®Visual inspection was conducted before packaging in 2000. exceptFor the sealing test, we also randomly sample each batch of products for the following tests to ensure strict compliance with Sartorius Stedim Biotech's internal quality assurance standards:
-Shell burst pressure test
-Voltage withstand test
-Bubble point test
-Aseptic filtration performance
-Flow rate test
-Sterilization test.
Performance: Diameter size is only 64mm, Midisart®The filtration area of 2000 is 20 cm ², which also means it has high flow rate performance! Midisart®The filtering performance of 2000 is far more than that. They can withstand at least 20 rounds of high-pressure sterilization at 134 ° C!
Chemical compatibility: Midisart®The materials used in 2000 (PTFE and polypropylene) have good compatibility with solvents and other chemicals. However, its compatibility may also vary due to various factors such as temperature, concentration, composition, etc. Therefore, we suggest that you conduct an experiment to test Midisart®Is 2000 compatible with the special media you want to filter. Midisart®2000 can also be used for filtering aqueous solutions. In this case, alcohol wetting must be used first to overcome the hydrophobicity of the membrane.
Midisart ® 2000 individually packaged, pre disinfected.
Connect now!
Midisart ® 2000 can conduct integrity testing and provide reproducible results. The natural hydrophobic PTFE material can effectively remove moisture. Enhanced stability through polypropylene mesh, with a pressure resistance of up to 3 bar (approximately 44 psi). In addition, due to Midisart ® 2000 All materials have passed the current USP Plastic VI standard testing, therefore they have biological safety. Midisart ® 2000 can easily withstand at least 20 high-pressure sterilization cycles without any loss in performance. Every Midisart ® The 2000 UPN encoding box provides convenient memory cartridges to record each high-pressure sterilization cycle through labeling or cutting. This feature is key to complying with GLP and ISO standards regarding document traceability.
The casing of each component undergoes 100 automatic integrity tests, and the sealing of the membrane during manufacturing is part of the product quality control testing. -To ensure product quality, the production batch number and product serial number are printed on the outer shell of each filter. Midisart ® Visual inspection was conducted before packaging in 2000. In addition to the sealing test, we also randomly sample each batch of products for the following tests to ensure strict compliance with Sartorius Stedim Biotech's internal quality assurance standards:
Shell burst pressure test
Withstand Voltage Test
Bubble point test
Pyrogen test
Aseptic filtration performance
flow velocity test
Aseptic testing
The diameter size is only 64mm, Midisart®The filtration area of 2000 is 20 cm ², which also means it has high flow rate performance! Midisart®The filtering performance of 2000 is far more than that. They can withstand at least 60 rounds of high-pressure sterilization at 134 ° C!
| type | air filter |
| branch company | Pharmaceutical/Biotechnology |
| Filter type | Flat disc bag filter |
| filtration area | 20 cm² |
| Membrane filter material | PTFE |
| aperture | 0,2 µm |
| Filter material | Polytetrafluoroethylene (PTFE) |
| housing material | Polypropylene (PP) |
| bacterial retention | According to the ASTM method, 1 x E7 CFU/square centimeter defective shortwave fungus ATCC ® Quantity interception of 19146 |
| bacterial endotoxin | Tested by LAL<0.18 EU/mL |
| Extract material | The product meets or exceeds the current USP quality standard for "sterile water for injection". |
| 生物安全性 | All components of the filter are made of materials that have passed the current USP plastic grade VI biological reaction test (whole-body injection, intradermal, and implant tests). |
| sterilization | High pressure sterilization: 20 times more, 134 ℃ higher, 2 bar | 29 psi |
| No fiber dissolution | This product complies with Title 21 of the Code of Federal Regulations (CFR), Sections 210.3 (b) (6) and 211.72 |
| GMP compliance | The production of this product complies with current Good Manufacturing Practice (cGMP) standards. |
| Z high operating pressure | 3 bar |
| Packing Specification | 12 |
| membrane material | Polytetrafluoroethylene (PTFE) |
| Connector import | Hose hook |
| Connector outlet | Hose hook |