5D44
NovaSeptum® GO Conical Tube Sampling Unit, Manifold (5-valve) with Dip Tube and Inlet C-Flex® Tubing
sterile; γ-irradiated, volume × volume 15 mL × 50 mL
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Quality Level
material
TPE tubing (Inlet C-Flex), polycarbonate Luer lock, polypropylene clip (TTP clip), polypropylene tube (Fluid contact layer (conical tube)), polystyrene tube (Fluid contact layer (conical tube))
agency
according to ISO 11137 (sterilization), according to ISO Clean Room Class 8 conditions in a facility, certified by the ISO 14644-1 standards, meets USP 88 biological reactivity (all component materials)
sterility
sterile; γ-irradiated
product line
NovaSeptum® GO
feature
autoclavable: no
parameter
max. pressure at 0.50 bar (7.25 psi), 2-60 °C temp. range (36-140 °F)
volume × volume
15 mL × 50 mL
application(s)
cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pharma/biopharma processes
sterile sampling
viral therapy
storage temp.
2-30°C
General description
For those samples that need to be transferred between containers, the standard dip tube reaches to the bottom of the tube enabling easy aseptic transfer while minimizing product loss and foaming. When used in a single-use manufacturing process, a weldable option with C-Flex® tubing is available.
The NovaSeptum® GO Conical Tube Sampling Unit offers you flexibility while minimizing the risk of both product and process contamination.
Application
Features and Benefits
Packaging
Other Notes
Fluid contact layer (conical tube&dip tube): Polystyrene, dip tube: LDPE (Low density polyethylene pharmalene FL20PH)
Insert Inox 316L
TTP clip Polypropylène
Tubing: Thermoplastic elastomer (TPE), Inlet C Flex
Outlet Tubing: Female and male Luer-Lok®
Legal Information
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Este artículo | |||
|---|---|---|---|
| product line NovaSeptum® GO | product line NovaSeptum® GO | product line NovaSeptum® GO | product line NovaSeptum® GO |
| material TPE tubing (Inlet C-Flex), polypropylene clip (TTP clip), polystyrene tube (Fluid contact layer (conical tube)), polycarbonate Luer lock, polypropylene tube (Fluid contact layer (conical tube)) | material TPE tubing (Inlet C-Flex), polycarbonate Luer lock, polypropylene clip (TTP clip), polypropylene tube (Fluid contact layer (conical tube)), polystyrene tube (Fluid contact layer (conical tube)), tubing (Female and male Luer-Lok®) | material TPE tubing (Inlet C-Flex), polycarbonate Luer lock, polypropylene clip (TTP clip), polypropylene tube (Fluid contact layer (conical tube)), polystyrene tube (Fluid contact layer (conical tube)), tubing (Female and male Luer-Lok®) | material 316 stainless steel cannula (ASTM®), polyester body, polypropylene clip (TTP clip), polypropylene tube (Fluid contact layer (conical tube)), polystyrene tube (Fluid contact layer (conical tube)), silicone septum ( Platinum-cured), tubing (Female and male Luer-Lok®) |
| parameter max. pressure at 0.50 bar (7.25 psi), 2-60 °C temp. range (36-140 °F) | parameter max. pressure at 0.50 bar (7.25 psi), 2-60 °C temp. range (36-140 °F) | parameter max. pressure at 0.50 bar (7.25 psi), 2-60 °C temp. range (36-140 °F) | parameter max. pressure at 0.50 bar (7.25 psi), 2-50 °C temp. range (36-112 °F) |
| sterility sterile; γ-irradiated | sterility sterile; γ-irradiated | sterility sterile; γ-irradiated | sterility sterile; γ-irradiated |
| application(s) cell therapy | application(s) cell therapy | application(s) cell therapy | application(s) cell therapy |
| agency according to ISO 11137 (sterilization), certified by the ISO 14644-1 standards, according to ISO Clean Room Class 8 conditions in a facility, meets USP 88 biological reactivity (all component materials) | agency according to ISO 11137 (sterilization), according to ISO Clean Room Class 8 conditions in a facility, certified by the ISO 14644-1 standards, meets USP 88 biological reactivity (all component materials) | agency according to ISO 11137 (sterilization), according to ISO Clean Room Class 8 conditions in a facility, certified by the ISO 14644-1 standards, meets USP 88 biological reactivity (all component materials) | agency according to ISO 11137 (sterilization), according to ISO Clean Room Class 8 conditions in a facility, certified by the ISO 14644-1 standards, meets USP 88 biological reactivity (all component materials) |
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