可焊接生物制药软管 CJFLEXBIO TH
半透明软管,硬度61A,(可定制50A和69A),可无菌焊接,生物制药用,600RPM转速下蠕动泵连续使用寿命500小时,流量变化在7%以内,是第一款超过500小时的可焊接生物制药用蠕动泵管用软管
应用范围:
细胞培养基、细胞发酵
诊断设备、实验室研究
药品生产、疫苗生产、试剂配制
植物产品生产
蠕动泵管段
无菌灌装和配药系统
产品特点:
1.超高焊接强度,可进行热封口或热焊接
2. 不致热、无热源无细胞毒性,非溶血,生物兼容性好
3.内壁超光滑,低血小板粘附率,低蛋白质结合率,低析出物,可渗透性明显低于硅胶
4. 耐浓酸和浓碱
5.在-45~+135C范围内均可维持高弹性
6.可辐射灭菌、EO灭菌
7. ISO7级洁净间生产,符合FDA、USP VI等标准,严格遵循GMP指南制造
8.可通过焚烧进行安全处理
CJFLEX TH is a translucent tube with hardness of 61A (can be customized for 50A and 69A). It can be aseptically welded for biopharmaceuticals. The peristaltic pump has a continuous service life of 500 hours at 600 RPM, and the flow rate changes within 7%. It is the first weldable peristaltic pump hose for biopharmaceutical use over 500 hours.
Application:
Cell
culture medium and cell fermentation
Diagnostic
equipment, laboratory research
Drug
production, vaccine production, reagent preparation
Production
of plant products
Peristaltic
pump pipe section
Aseptic
filling and dispensing system
Features/Benefits:
编码
对应蠕动泵号
内径*外径(mm)
颜色
单卷长度(ft)
TH00100030
-
1.00*3.00
半透明
50
TH00150033
-
1.50*3.3
半透明
50
TH00200038
-
2.06*3.76
半透明
50
TH00200040
-
2.00*4.00
半透明
50
TH00200041
-
3.00*5.00
半透明
50
TH00160048
14#
1.59*4.76
半透明
50
TH00480096
15#
4.76*9.53
半透明
50
TH00320064
16#
3.18*6.35
半透明
50
TH00640096
17#
635*9.53
半透明
50
TH00790111
18#
7.94*11.11
半透明
50
TH00640112
24#
6.35*11.11
半透明
50
TH00480080
25#
4.76*7.94
半透明
50
TH00400072
-
4.00*7.20
半透明
50
TH00640127
26#
6.35*12.70
半透明
50
TH00790127
35#
7.94*12.70
半透明
50
TH00960144
36#
9.53*14.29
半透明
50
TH00960160
73#
9.53*15.88
半透明
50
TH01270191
82#
12.70*19.05
半透明
50
Super
high welding strength, can be used for hot sealing or welding
No
heat, no heat source, no cytotoxicity, no hemolysis, good biocompatibility
The
inner wall is super smooth, with low platelet adhesion rate, low protein
binding rate, low precipitate, and its permeability is significantly lower than
that of silica gel
Strong
acid and alkali resistance
High
elasticity can be maintained in the range of - 45℃ to +135℃
It
can be sterilized by radiation and EO
ISO
7 clean room production, in line with FDA, USP VI and other standards, in
strict accordance with GMP guidelines
It
can be safely treated by incineration
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