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E461-90020

NovaSeptum® GO Sampling System; Accurate Volume Application

20mL

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UNSPSC Code:
41104105
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Quality Segment

material

316 stainless steel cannula, polycarbonate syringe (fluid contact layer), polyester body, silicone septum (platinum-cured), silicone syringe (medical fluid contact layer; platinum cured silicone), silicone tubing

agency

ISO 10993-5 (all component materials), USP 87 Cytotoxicity Elution Test (In Vitro), according to ISO 11131 (sterilization), according to ISO 146441, meets the criteria for Biological Reactivity Testing: can be any one or a combination of the following test methods USP<88> Systemic Injection Test (In Vivo)

sterility

sterile; β-irradiated

product line

NovaSeptum® GO

feature

autoclavable

parameter

-80-121 °C temp. range (-112-250 °F), 0.50 bar max. pressure (7.25 psi)

impurities

<2.15 EU/device bacterial endotoxins (LAL test)

fitting

female Luer-Lok® outlet, male Luer-Lok® outlet

application(s)

cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pathogen testing
pharma/biopharma processes
pyrogen testing
sterile sampling
sterility testing
viral therapy

storage temp.

10-30°C

General description

Device configuration: single unit sampling
NovaSeptum® GO Accurate Volume Syringes are designed to take samples from 1 mL to 20 mL, enabling operators to directly dispense sample products with milliliter accuracy. The ability to accurately measure the sample taken is particularly important for sampling of high value products and reduces expensive product waste. For sterility testing, pyrogenic testing, endotoxin testing, chemical analysis, pH analysis and fermentation applications. The syringes are ideal for storage. A closed, sterile sampling method can significantly reduce risk of cross contamination. Ideal for sampling from aseptic and sterile processes, the NovaSeptum® GO sterile sampling system provides consistently representative samples, safely and securely.

Application

Sterility testing, pyrogenic testing, endotoxin testing, chemical analysis, pH analysis, and fermentation applications

Packaging

40 units per box

Preparation Note

Units are integrity tested at regular intervals during manufacturing.

Aqueous extraction contains < 2.15 EU per device as determined using the Limulus Amebocyte Lysate (LAL) test.

Other Notes

  • Septum: Platinum-cured silicone
  • Body: Polyester
  • Cannula: ASTM® 316 L Stainless steel
  • Fluid contact layer (syringe): Polycarbonate, platinum-cured silicone, medical silicone fluid
  • Tubing: Silicone
  • Outlet Tubing: Female and male Luer-Lok®

Legal Information

ASTM is a registered trademark of American Society for Testing and Materials
Luer-Lok is a registered trademark of Becton-Dickinson & Co.
NOVASEPTUM is a registered trademark of Merck KGaA, Darmstadt, Germany

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Este artículo
E46490005E46490020E46190005
description

20mL

description

5x5mL

description

5x20mL

description

5mL

fitting

male Luer-Lok® outlet, female Luer-Lok® outlet

fitting

female Luer-Lok® outlet, male Luer-Lok® outlet

fitting

male Luer-Lok® outlet, female Luer-Lok® outlet

fitting

male Luer-Lok® outlet, female Luer-Lok® outlet

product line

NovaSeptum® GO

product line

NovaSeptum® GO

product line

NovaSeptum® GO

product line

NovaSeptum® GO

agency

according to ISO 11131 (sterilization), meets the criteria for Biological Reactivity Testing: can be any one or a combination of the following test methods USP<88> Systemic Injection Test (In Vivo), according to ISO 146441, USP 87 Cytotoxicity Elution Test (In Vitro), ISO 10993-5 (all component materials)

agency

meets the criteria for Biological Reactivity Testing: can be any one or a combination of the following test methods USP<88> Systemic Injection Test (In Vivo), according to ISO 146441, USP 87 Cytotoxicity Elution Test (In Vitro), ISO 10993-5 (all component materials), according to ISO 11137 (sterilization)

agency

according to ISO 146441, meets the criteria for Biological Reactivity Testing: can be any one or a combination of the following test methods USP<88> Systemic Injection Test (In Vivo), according to ISO 11137 (sterilization), ISO 10993-5 (all component materials), USP 87 Cytotoxicity Elution Test (In Vitro)

agency

according to ISO 11131 (sterilization), according to ISO 146441, ISO 10993-5 (all components materials), meets the criteria for Biological Reactivity Testing: can be any one or a combination of the following test methods USP <88> Systemic Injection Test (In Vivo), USP 87 Cytotoxicity Elution Test (In Vitro)

material

316 stainless steel cannula, polyester body, polycarbonate syringe (fluid contact layer), silicone septum (platinum-cured), silicone syringe (medical fluid contact layer; platinum cured silicone), silicone tubing

material

polyester body, 316 stainless steel cannula, polycarbonate syringe (fluid contact layer), PureFlex™ polyethylene bag (Drainage bag), silicone septum (platinum-cured), silicone tubing, silicone syringe (medical fluid contact layer; platinum cured silicone)

material

316 stainless steel cannula, PureFlex™ polyethylene bag (Drainage bag), polyester body, silicone syringe (medical fluid contact layer; platinum cured silicone), silicone septum (platinum-cured), polycarbonate syringe (fluid contact layer), silicone tubing

material

316 stainless steel cannula, silicone tubing, silicone septum (platinum-cured), polycarbonate syringe (fluid contact layer), silicone syringe (medical fluid contact layer; platinum cured silicone), polyester body

storage temp.

10-30°C

storage temp.

10-30°C

storage temp.

10-30°C

storage temp.

10-30°C

application(s)

cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pathogen testing
pharma/biopharma processes
pyrogen testing
sterile sampling
sterility testing
viral therapy

application(s)

cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pathogen testing
pharma/biopharma processes
pyrogen testing
sterile sampling
sterility testing
viral therapy

application(s)

cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pathogen testing
pharma/biopharma processes
pyrogen testing
sterile sampling
sterility testing
viral therapy

application(s)

cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pathogen testing
pharma/biopharma processes
pyrogen testing
sterile sampling
sterility testing
viral therapy


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