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Eppendorf™ epTIPS Box IVD
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Artikelnummer. 17302930 Shop alle Eppendorf produkter
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Volumen (metrisk):
50 to 1000 μL
Farvekode:
Blue
Mængde:
480 Pk.
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Artikelnummer. 17302930

Brand: Eppendorf™ 0030076540

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epT.I.P.S. pipette tips are designed to enable minimal insertion and ejection force and maximum tightness in system with Eppendorf pipettes.

  • epT.I.P.S.™ Box 2.0 (EU-IVD), Eppendorf Quality™
  • Contamination-free transfer of trays to stable working box
  • System optimized for use with multichannel pipettes
  • Color-coded trays for simple identification of tips and pipette
  • Tips can be attached to pipette from refill trays
  • The trays and boxes can be autoclaved at 121 °C for subsequent use
  • The pipette tips of the epT.I.P.S.™ product group with the respective product numbers are designed and constructed for low-contamination transfer of liquids, in particular for samples from the human body and for reagents within the scope of an in-vitro diagnostic application in order to allow the in-vitro diagnostic medical device to be used as intended. The above mentioned epT.I.P.S.™ are in-vitro diagnostic devices according to Directive 98/79/EC of the European Parliament and the Council dated October 27, 1998. They are intended exclusively for single use and for application by qualified staff.
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Tekniske data

Volumen (metrisk) 50 to 1000 μL
Filtreret Non-filtered
Farve Colorless
Autoklaverbar Autoclavable
Længde (metrisk) 71 mm
Certificeringer/compliance 98/79 EC
Rene krav Eppendorf Quality™
Emballage Set
Mængde 480 Pk.
Produkttype Consumables
Farvekode Blue
Engangs Single-use
Produktlinje epT.I.P.S.
Materiale Polypropylene
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The pipette tips of the epT.I.P.S.™ product group with the respective product numbers are designed and constructed for low-contamination transfer of liquids, in particular for samples from the human body and for reagents within the scope of an in-vitro diagnostic application in order to allow the in-vitro diagnostic medical device to be used as intended. The above mentioned epT.I.P.S.™ are in-vitro diagnostic devices according to Directive 98/79/EC of the European Parliament and the Council dated October 27, 1998. They are intended exclusively for single use and for application by qualified staff.

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