详细介绍:
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TPEE 日本东丽 7247M HB582特性:
TPEE 日本东丽 其他型号报价:
TPEE
|
日本东丽
|
6347
|
15000
|
TPEE
|
日本东丽
|
6347A
|
22000
|
TPEE
|
日本东丽
|
7247
|
23000
|
TPEE
|
日本东丽
|
7247M
|
23000
|
TPEE
|
日本东丽
|
7247M HB582
|
40000
|
TPEE
|
日本东丽
|
7247R-F
|
48000
|
TPEE
|
日本东丽
|
7247W
|
35000
|
TPEE
|
日本东丽
|
7277
|
23000
|
TPEE
|
日本东丽
|
G3548L
|
26500
|
TPEE
|
日本东丽
|
HDT576
|
40000
|
TPEE
|
日本东丽
|
HTC2551W
|
40000
|
TPEE
|
日本东丽
|
HTC2751
|
39000
|
TPEE
|
日本东丽
|
SB704W BK
|
30000
|
TPEE 日本东丽 7247M HB582 :2017年4月24日,日本东丽公司发布消息称,东丽公司5种聚酯纤维、尼龙面料的超强性能再次获得日本宇宙航空研究开发所(JAXA)的高度评价,并通过JAXA创立的JAXACOSMODE品牌认证。
此次通过JAXACOSMODE品牌认证的5种材料分别是具有极高舒适伸展性能的PRIMEFLEX?、强力吸汗速干的FIELDSENSOR?、耐脏易清洁的TECHNOCLEAN?、具有防静电功能的SUPERPAREL?以及带超高导电性能的纤维材料LUANA?。这些材料改善了航空舱内宇航员们着装的舒适性和安全性,受到日本宇宙航空研究开发机构的高度评价。此次通过JAXACOSMODE品牌的认证,无疑将再次推动航空技术民用化的进程。东丽公司表示,今后采用这5种材料生产的商品将会附上JAXACOSMODE的标签,也会在店铺介绍中详细标识出来。东丽公司预计此类商品2017年销售额为1.2亿日元,2020年计划达到3.5亿日元。
据悉,JAXACOSMODE是日本宇宙航空研究开发机构(JAXA)与民间拥有尖端技术的企业合作开发的商品品牌,2008年由JAXA创立,旨在在日常生活中向人们传达宇宙与天空的魅力。东丽早在2012年就与JAXA合作开发出具有除臭功能的新面料MONSIEUR—ON?,也已获得JAXACOSMODE品牌认证。东丽意欲在长期经营目标“AP-GrowthTORAY2020”中,进一步树立世界尖端材料厂商形象,利用高分子化学、有机合成化学等领域的核心技术加速开发超高性能的尖端新材料。
TPEE 日本东丽 7247M HB582 :oray Industries, Inc. (head office:
Chuo-ku, Tokyo; President: Akihiro Nikkaku; hereinafter referred to as
"Toray") today announced that on March 30, 2017 it received approval
for an additional orally disintegrating tablets formulation (REMITCH® OD Tablets 2.5 μg; hereinafter referred to as the
"OD tablets") of REMITCH® CAPSULES 2.5 μg. Toray
already has manufacturing and marketing approval for the drug, which is being
distributed by Torii Pharmaceutical Co., Ltd. (head office: Chuo-ku, Tokyo; President:
Shoichiro Takagi; hereinafter referred to as "Torii Pharmaceutical")
as a treatment of pruritus in hemodialysis and chronic liver disease patients
(use only when sufficient efficacy is not obtained with the existing therapies
or treatments) in Japan (tie-up with Japan Tobacco Inc. (head office:
Minato-ku, Tokyo; President: Mitsuomi Koizumi)) and is being promoted by
Sumitomo Dainippon Pharma Co., Ltd. (head office: Osaka; President: Masayo
Tada; hereinafter referred to as "Sumitomo Dainippon Pharma") for
treating pruritus in chronic liver disease patients. The OD tablets, for which
Toray has obtained the approval this time, can be taken with or without water
and therefore is convenient for the patients whose swallowing capabilities have
deteriorated or those who have restrictions on water intake and is expected to
lead to improved drug intake compliance.
The four companies expect that the approval of additional formulation
would offer a new treatment option and significantly contribute to the treatment
of pruritus in hemodialysis and chronic liver disease patients. The outline of REMITCH® OD Tablets 2.5μg is as
follows:
[Product
outline]
|
Product
name
|
:
|
REMITCH® OD
Tablets 2.5μg
|
Generic
name
|
:
|
Nalfurafine
hydrochloride
|
Indications
|
:
|
Improvement
of pruritus in the following patients (use only when sufficient efficacy is
not obtained with the existing therapies or treatments): hemodialysis
patients, patients with chronic liver disease
|
Dosage
and administration
|
:
|
The
recommended dose for adults is 2.5μg of nalfurafine
hydrochloride once daily, administered orally after an evening meal or before
bedtime. The dose can be increased in accordance with the symptoms, the
maximum dose is 5μg once daily
|
Date
of approval for the additional formulation : March 30, 2017
|
Manufacturer/distributor
|
:
|
Toray
Industries, Inc.
|
|
|
|
REMITCH® OD
Tablets 2.5μg
The
agent is the world’s first highly selective kappa opioid receptor agonist developed
by Toray and has been distributed in Japan since March 2009 by Torii
Pharmaceutical as a treatment for pruritus in hemodialysis patients. It
controls itching based on a mechanism that is different from antihistamines
and anti-allergy drugs and, therefore, was developed with the expectation
that it would be effective for pruritus which could not be controlled with
existing treatments. In addition, REMITCH® was also
approved for treating pruritus in chronic liver disease patients in May 2015,
and Sumitomo Dainippon Pharma formed an alliance promoting it for this
indication.
The
agent had been available only as a soft capsule until now. Toray had been
developing the OD tablets version, which can be administered without water,
so as to improve convenience for patients whose swallowing capabilities have
deteriorated or those who have restrictions on water intake.
|
如需了解更多关于TPEE 日本东丽 7247M HB582及 的详细信息,欢迎致电联系。
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TPEE 日本东丽 7247M HB582今日新闻:
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