Lifemeta™ DCF Aseptic Disconnector 5/pk
Regular price
$123.20 USD
Regular price
$176.00 USD
Sale price
$123.20 USD
(-30%)
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*Ships within 3 Business Days
*Read our Shipping Policy and Refund Policy
*Read our Shipping Policy and Refund Policy
*Not for medical use
Lifemeta™ DCF aseptic disconnector is mainly used for sterile disconnection of different stages in biopharmaceutical processes, especially in upstream and formulation filling. After disconnection, the Alloy C-276 spring automatically closes to realize the fluid path sealing, and prevent microorganisms entering the fluid path during disconnection.
Lifemeta™ DCF aseptic disconnector main body includes a thumb latch, which is simple and convenient to operate. With an easy push of the connector thumb latch, sterile disconnection can be achieved. The connector can realize sterile disconnection in any environment.
Specifications
| Materials | Main Body | Polysulfone(PSF) |
| Flow Path Springs | Alloy C-276 | |
| O-rings | Silicone | |
| Physical Properties | Temperature Range | -80~138°C |
| Pressure Range | Up to 6.9 bar | |
| Vacuum Resistance | Up to 1.0 bar | |
| Sterilization | Can be sterilized by gamma irradiation at 25-45kGy or autoclaved for 60 minutes at 130 °C |
|
| Package | Delivery Condition | Non-sterile/Sterile Individually Packed |
| Pack Size | 5/pk | |
Features
- Can realize sterile disconnection in any environment
- Simple and intuitive operation with one-step quick disconnection
- Automatic shutoff valves to realize safe seal
- Equipped with sealing cap and plug, double layer protection, reduce the risk of leakage
- No requirement for additional equipment to make sterile disconnection
Applications
- Sterile disconnection after sampling
- Sterile disconnection after inoculation of bioreactor
- Sterile disconnection of tubing in different cleanrooms
- Sterile disconnection after each production process
Quality Assurance
- Validation guide are available
- Extractables and leachables report are available on request
- Resin raw material meets the requirement of USP <87> in Vitro Biological Reactivity Test
- Resin raw material meets the requirement of USP <88> Biological Reactivity Test, in Vivo for Class VI plastics
- Aqueous extraction contains < 0.25 EU/mL as determined by Amebocyte Lysate, USP <85>
- Particulate matter in the product eluent meets the requirements in USP<788> for large volume parenterals
- ISO 9001:2015 Quality Management System
- ADCF raw materials
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