推荐产品
物料
PureFlex™ polyethylene bag (film)
polyester body
silicone septum (platinum-cured)
silicone tubing
stainless steel body (ASTM® 316 L)
质量水平
Agency
according to ISO ISO 11137
meets USP 88 Biological Reactivity
无菌性
sterile; β-irradiated
产品线
NovaSeptum® GO
特点
autoclavable
参数
-20-125 °C temp. range (-4-257 °F)
0.30 bar max. pressure (4.35 psi)
杂质
<2.15 bacterial endotoxins (LAL test, EU/device)
配件
male Luer-Lok® outlet (with female sterile vent filter)
应用
cell therapy
gene therapy
life science and biopharma
mAb
ophthalmics
parenterals
pharma/biopharma processes
sterile sampling
viral therapy
储存温度
room temp
一般描述
A range of NovaSeptum® GO small pack size kits available to trial a sterile sampling solution for your process. Choose from several collection container types: high purity bags, autoclavable bags, bottles or accurate volume syringes (5 containers per pack). The 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. 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. Autoclavable bags are intended for applications where the unit is connected to a vessel that needs to be sterilized by autoclave. Bio-neutral plastic bottles or high purity bags are ideal for all tests and are available in a range of sizes. Use a trial kit in combination with a NovaSeptum® GO holder.
应用
Sterile sampling
Sterility testing, pyrogenic testing, endotoxin testing, chemical analysis, pH analysis, and fermentation applications
包装
5x autoclavable bag 250ml
组分
- Septum: Platinum-cured silicone; Body: Polyester
- Cannula: ASTM® 316 L Stainless steel
- Fluid contact layer (bag): Polypropylene film
- Tubing: Silicone
- Outlet Tubing: Male Luer-Lok® with female sterile vent filter
制备说明
All component materials, in contact with sampling liquid, meet the criteria for Class VI testing based on USP <88> Biological Reactivity, in vivo.
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.
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.
Assembled under ISO Clean Room Class 8 conditions in a facility certified to ISO 14644-1 standards.
法律信息
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
PUREFLEX is a trademark of Merck KGaA, Darmstadt, Germany
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