推荐产品
材料
316 stainless steel cannula
PureFlex™ polyethylene bag (drainage bag)
TPE tubing
polyester body
polyethylene bottle (fluid contact layer)
silicone septum (platinum-cured )
品質等級
agency
according to ISO 11137 (sterilization)
certified by the ISO 146441
meets USP 88 biological reactivity (all component materials)
無菌
sterile; γ-irradiated
產品線
NovaSeptum® GO
特點
autoclavable: no
參數
-80-50 °C temp. range (-112-122 °F)
0.30 bar max. pressure (4.35 psi) at ±25 °C
雜質
<2.15 EU/device bacterial endotoxins (LAL test)
應用
bioburden testing
cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pathogen testing
pharma/biopharma processes
sterile sampling
viral therapy
儲存溫度
room temp
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一般說明
Device configuration: Multi-sampling
The NovaSeptum® GO bottle sampling unit is intended for applications where high purity, such as low endotoxin levels, is required. This sampling unit is available with a 2 mm needle and must be used with a NovaSeptum® GO holder. The bio-neutral plastic bottles are ideal for all tests and available in a range of sizes. 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.
應用
Endotoxin
Bioburden - Archiving
Bioburden - Archiving
包裝
E874-80060 (5x60 ml bottles, 5 units per box)
E874-80125 (5x125 ml bottles, 4 units per box)
E874-80250 (5x250 ml bottles, 3 units per box
E874-80125 (5x125 ml bottles, 4 units per box)
E874-80250 (5x250 ml bottles, 3 units per box
成分
- Septum: Platinum-cured silicone
- Body: Polyester
- Cannula: ASTM® 316 L Stainless steel
- Fluid contact layer (bottle): Polyethylene Terephtalate Glycol
- (Drainage bag): PureFlex™ Polyethylene filmfilm)
- Tubing: Thermoplastic elastomer (TPE)
- Outlet Tubing: Cap
準備報告
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.
Aqueous extraction contains < 2.15 EU per device as determined using the Limulus Amebocyte Lysate (LAL) test.
法律資訊
ASTM is a registered trademark of American Society for Testing and Materials
NOVASEPTUM is a registered trademark of Merck KGaA, Darmstadt, Germany
PUREFLEX is a trademark of Merck KGaA, Darmstadt, Germany
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