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XC 47/11-10
The MVE XC 47/11-10 Bio dewar vessel provides storage of 5000 straws and 1050 vials. These durable and lightweight vessels are manufactured to the highest global standards, protected by the industry's longest 5-year vacuum system warranty, and can be used in difficult operating conditions.
Distinctive features:
- Designed for storing a small number of samples
- Low liquid nitrogen consumption
- Convenient lightweight packaging
Spare parts warranty 2 years * Vacuum system warranty 5 years
| Maximum storage capacity | |
| Number of canisters | 10 |
| The number of 1/2 ml straws 10/cane | 3200 |
| The number of 1/2 ml straws on 1 level bulk | 5000 |
| The number of 1/2 ml straws on 2 level bulk | - |
| The number of 1,2 and 2,0 ml vials 5/cane | 1050 |
| The number of 1,2 and 2,0 ml vials 5/ rack | - |
| Performance | |
| Volume of liquid nitrogen nitrogen without storage system up to star-shaped structure, calculated | 47,4 l |
| Volume of liquid nitrogen for filling cryopreservation facilities without a storage system up to the star-shaped design, the calculated | - |
| Static evaporation rate* | 0,39 l/day |
| Working duration** | 76 full days |
| Unit dimensions | |
| Inner diameter of the neck | 127 mm |
| Overall height | 673 mm |
| Overall internal height | - |
| Outer diameter | 508 mm |
| Canister height | 279 mm |
| Canister diameter | 71 mm |
| Distance: platform to top of neck | - |
| Weight empty | 19,0 kg |
| Weight full | 54,6 kg |
* The static loss rate and the static offline storage rate are nominal. The actual values will depend on the nature of the use of the tank, atmospheric conditions and production tolerances.
** Operating time (time of complete evaporation of liquid nitrogen) - an arbitrary value for evaluating the performance of the system under normal operating conditions for storing samples in the liquid phase. The actual value may vary depending on the current atmospheric conditions, the condition of the cryogenic storage facility, production tolerances, and the nature of operation.
Complies with MDD 93/42/EEC, the EU Medical Equipment Directive.
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