CryoPure tubes, 2 ml, QuickSeal screw cap, white

Order number: 72.379
CryoPure tubes, 2 ml, QuickSeal screw cap, white

Product description

Order number 72.379
Product description CryoPure tubes, 2 ml, tube: PP, QuickSeal screw cap, cap assembled, HD-PE, white, external thread, nominal volume: 1.8 ml, Cryo Performance Tested, 50 piece(s)/bag

Product characteristics

Label/ Print with print
Colour of print/label white
Graduation yes
Cap QuickSeal screw cap
Closure type screw cap
Internally or externally threaded cap external thread
Volume of work 1,8 ml
Vessel type Tube


Sample volume 1.8 ml
Max. volume 2 ml
Diameter 12.65 mm
Length of product 46.7 mm
Length excluding cap 39.8 mm

Material & colours

Closure material High Density Polyethylene (HD-PE)
Colour of cap white
Tube material Polypropylene (PP)

Purity & certification

Product category In vitrodiagnostic device, CE
CE certified CE
Purity standard Cryo Performance Tested
Sterilisation Electron irradiation
Pyrogen-free yes
Non-cytotoxic yes
Batched yes


Minimum order qty. 500
Type of smallest subpackaging bag
Piece(s) / inner box 500
Piece (s) / outer case 2000
Piece(s) / pallet 104000
Depth of box 293 mm
Width of box 183 mm
Height of box 118 mm
Depth of case 598 mm
Width of case 378 mm
Height of case 135 mm
Case volume 0.0305 cbm
Weight of product 0.002 kg
Weight of case 5.14 kg
EAN of inner box 4038917081399
EAN case 4038917080552
Product specification


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    Where should the CryoPure tubes in the nitrogen tank be stored – in the liquid phase or in the gas phase?

    Because from -130°C no further biochemical reactions occur in the cells, storing these in the gas phase (< -130°C) is entirely sufficient for successful cryopreservation. We therefore recommend that CryoPure tubes are stored in the gas phase. Please note the safety advice included with our products. 

  • +

    How are the Sarstedt CryoPure tubes certified?


    As per DIN EN ISO 11137 – 'Sterilization of health care products – Validation and routine control for sterilization with radiation'


    Based on the LAL test as per the FDA guideline for medical devices, detection limit < 0.06 EU/ml


    In compliance with DIN EN ISO 10993 – 'Biological evaluation of medical devices – Part 5 Tests on in-vitro cytotoxicity'


    The evidence for estimating freedom from mutagens was gathered according to the Ames Test II

    IVD conformity confirmed

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