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1711-10050

NovaSeptum® High Purity Unit

High Purity Application; 50mL

Synonyma:

General sampling, high purity application, 50 mL, NovaSeptum® High Purity Unit

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Vám/Skladová položkaDostupnostCena
50 pkg

Očekávané datum odeslání09. června 2026odAreál Kühne+Nagel spol. s r.o.

82 200,00 Kč

O této položce

eCl@ss:
36101790
UNSPSC Code:
41104105

82 200,00 Kč


Očekávané datum odeslání09. června 2026podrobné informace


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Název produktu

NovaSeptum® General Sampling Unit; High Purity Application, 50mL

Quality Segment

material

316L stainless steel cannula (ASTM), polyester body, polyethylene bag (drainage), polyethylene bag (sampling), polyethylene tubing, silicone septum (medical grade platinum-cured)

needle size

1.0 mm

sterility

sterile

manufacturer/tradename

NovaSeptum®

parameter

-20-50 °C max. temp., 0.5 bar max. sampling pressure (7.25 psi), 50 mL sample volume

impurities

≤2.15 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)

fitting

inlet septum unit (with a 1 mm needle), Luer outlet fitting (3-piece)

storage temp.

10-30°C

General description

Single sampling your product is critical throughout the manufacturing process. An imprecise or false positive result can lead to quarantine, as well may also require a repeat of the analysis.

With the NovaSeptum® High Purity Unit, contamination is no longer a threat. Ideal for aseptic and sterile processes, the closed design ensures your sample will be isolated from point of sample to analysis. NovaSeptum® also allows for savings of precious materials with its compact, no dead leg, design.

The wide range of standard and custom connectors guarantees the ability to collect sample everywhere needed. The high purity sampling units are ideally suited for sterility testing, pyrogenic testing, endotoxin testing, chemical analysis, ph analysis, and fermentation applications, and applications requiring very low affinity for proteins, complex carbohydrates or small molecules. It is available as a flat bag for easy storage and hanging.

Application

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

Preparation Note

Sterilization Method
Beta Irradiation (e-beam) minimum 25 kGy according to ISO 11137 TIR No. 27

Other Notes

Please refer to the Animal Origin Statement

Legal Information

NOVASEPTUM is a registered trademark of Merck KGaA, Darmstadt, Germany

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Tato položka
1711-101001714-100501711-11000
material

316L stainless steel cannula (ASTM), polyethylene bag (drainage), polyethylene tubing, polyester body, silicone septum (medical grade platinum-cured), polyethylene bag (sampling)

material

316L stainless steel cannula (ASTM), polyester body, polyethylene bag (drainage), polyethylene bag (sampling), polyethylene tubing, silicone septum (medical grade platinum-cured)

material

316L stainless steel cannula (ASTM), polyester body, polyethylene bag, polyethylene tubing, silicone septum (medical grade platinum-cured)

material

316L stainless steel cannula (ASTM), polyester body, polyethylene bag (drainage), polyethylene bag (sampling), polyethylene tubing, silicone septum (medical grade platinum-cured)

fitting

inlet septum unit (with a 1 mm needle), Luer outlet fitting (3-piece)

fitting

inlet septum unit (with a 1 mm needle), Luer outlet fitting (3-piece)

fitting

inlet septum unit (with a 1 mm needle), Luer outlet fitting (3-piece)

fitting

inlet septum unit (with a 1 mm needle), Luer outlet fitting (3-piece)

sterility

sterile

sterility

sterile

sterility

sterile

sterility

sterile

parameter

-20-50 °C max. temp., 50 mL sample volume, 0.5 bar max. sampling pressure (7.25 psi)

parameter

-20-50 °C max. temp., 0.5 bar max. sampling pressure (7.25 psi), 100 mL sample volume

parameter

-20-50 °C max. temp., 0.5 bar max. sampling pressure (7.25 psi)

parameter

-20-50 °C max. temp., 0.5 bar max. sampling pressure (7.25 psi), 1 L sample volume

needle size

1.0 mm

needle size

1.0 mm

needle size

1.0 mm

needle size

1.0 mm

impurities

≤2.15 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)

impurities

≤2.15 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)

impurities

≤2.15 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)

impurities

≤2.15 EU/mL bacterial endotoxins (LAL test, Aqueous extraction)


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