High Quanlity Infusion Set with Ce&ISO Certification

High Quanlity Infusion Set with Ce&ISO Certification

高质量输液器具有Ce&ISO认证

100000+
0.08 USD

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型号。 输液器
材料 PVC
环氧乙烷灭菌 环氧乙烷灭菌
成人
医疗器械监管类型 类型3
Jmd或OEM
ISO证书 iso13485,iso9001
运输包装 PE或吸塑
起源 中国常州
类型 输液器
证明 ce,sgs,iso13485
质量保证期 5年
标志印刷 使用徽标打印
医疗器械注册/记录号 Gxzz20153661379
证书 ce,iso,gmp
商标 jmd或oem
规范 ce,iso,gmp
HS编码 90183900

高品质输液套件采用CE和ISO认证ation

类型 输液器
材料 PVC
证明 ce,sgs,iso13485
消毒 环氧乙烷
质量保证期 3年
PE或吸塑
规范 ce,iso,gmp
管材料 pvc /非pvc
特征 一次性
有无针
S型 Luer Slip或Luer锁
管长 1.5m或OEM
组件 塑料钉
通风口 有/没有通风口
过滤 有/没有过滤器




特征
1.静脉插管:由不锈钢AISI 304制成,直径和长度根据ISO标准。列在表格中。
2.插管保护膜:由医用级PE制成,
3.双翼:采用医用PVC,注射塑料,足够柔软,根据AS 2485标准着色。
4.软管:由透明医用级PVC制成,软度足够,30厘米,60厘米,90厘米,长100厘米,外径2.50毫米,内
直径1.45mm。
鲁尔锁连接器:由透明硬PVC制成。
鲁尔锁盖:透明PVC制成。用线程机械
插管与机翼组合在一起。
8.管和翅膀,管和连接器用溶剂环己酮胶合。
吸塑:医用级胶凝纸(透析纸),塑胶膜。

规范:
1. EOG消毒,单次使用,无毒,无致热原
2.三次磨光的套管,抛光,这样做
注射无痛。
柔软的翅膀容易抓握,使固定变得容易。
4.用于识别套管直径的颜色代码(直径)
插管在翅膀上表示)

包装:
1.塑胶袋单独包装,100PCS /箱,2000PCS / CTN
吸塑包装,100PCS /箱,2000PCS / CTN

输液器 零件 MOQ
具有不同的型号 可以OEM要求 10万件
关于我们
江苏吉春医疗器械有限公司成立于1988年(原名郑路医疗材料厂),位于常州市肥沃的长江三角洲,省道232路经公司门口,方便交通便利的环境。 2008年,为了扩大生产规模,公司开始在郑路工业开发区征地,建成新厂房,现占地面积36000平方米,建筑面积18万平方米, 000个清洁车间面积5,500平方米。
公司主要从事单用医用聚合物医疗器械的开发,生产和销售。主要产品生产能力为:每年注射针数为10万套,年注射器6亿套,年输液量1亿套。公司环境优美,设备先进,设备齐全,各种先进的产品测量仪器和科学测试方法。公司生产的“吉春”品牌产品畅销全球,远销欧美,东南亚。客户对质量和服务的高度评价,合作伙伴和销售量不断增加。
公司拥有二十多年的发展历史,常州是老帝国城市,上海和南京经济特区的地理位置优越,具有独特的人文和地域优势,在注塑成型,自动化等方面发展自己的专业装配和包装。公司聘请高级管理人员,招聘了大量技术人员,建立了一套完整的质量管理体系。根据ISO 13485:2003 / YY / T0287-2003医疗器械质量管理体系要求,医疗器械良好的制造实践(试用),医疗器械良好的制造实践无菌医疗器械实施原则和检验评估标准出口),US21 CFR Part 820医疗器械目前良好的制造实践(cGMP),RDC59医疗器械良好的制造实践(GMP)和MDD 93/42 / EEC医疗器械指令,确保公司质量管理体系的实施和运行。
2001年,公司被中国医疗器械工业协会,中国护理协会和中国客户保障基金会评估为“质量标签企业的可靠生产”。 2002年公司通过ISO9002和CE认证,并于2004年通过了ISO9001 / ISO13485和CE认证。我们已经开创了一个发展中的道路,主导由一次性使用的医疗设备的精确制造。
在新世纪,吉春人将以市场为基础,展望未来,不断追求奋进。我们将通过创新的理念,技术和制度来寻求公司的发展,为人类健康做出贡献。

Model NO. infusion set
Material PVC
Ethylene Oxide Sterilization Ethylene Oxide Sterilization
Group Adult
Medical Device Regulatory Type Type 3
Brand Jmd or OEM
ISO Certificate ISO13485, ISO9001
Transport Package PE or Blister
Origin Changzhou, China
Type Infusion Set
Certification CE, SGS, ISO13485
Quality Guarantee Period 5 Years
Logo Printing With Logo Printing
Medical Devices Reg./Record No. Gxzz20153661379
Certificates Ce, ISO, GMP
Trademark JMD or OEM
Specification CE, ISO, GMP
HS Code 90183900

High Quanlity Infusion Set with CE&ISO Certificationationation

Type infusion set
Material PVC
Certification CE, SGS ,ISO13485
Sterilization Ethylene Oxide
Quality Guarantee Period 3 years
Package PE or Blister
Specification CE , ISO , GMP
Tube material PVC/Non- PVC
Feature Disposable
Needle with and without needle
stype Luer Slip or Luer lock
Tube length 1.5m or OEM
Components Plastic Spike
Air vent With / without air vent
Filter with / without filter




Features
1. Intravenous cannula: Made of Stainless steel AISI 304, diameter and Length according to the ISO standards. Listed in the table.
2. Cannula Protector: Made of Medical grade PE,
3. Double wings: Made of medical PVC, injection plastic, soft enough, Coloured according to the AS 2485 Standards.
4. Soft tube: Made of transparent medical grade PVC, soft enough, 30cm, 60cm, 90cm, 100cm in length, outer diameter 2.50mm, inner
Diameter 1.45mm.
5. Luer lock connector: Made of transparent, hard PVC.
6. Luer lock Cover: Made of transparent PVC. With thread. Mechanically
7. Cannula is assembled with wings together mechanically.
8. Tube and wings, tube and connector is glued with solvent Cyclohexanone.
9. Blister: Medical grade gelatinized paper(dialyse paper), plastic film.

Specification:
1. Sterilized by EOG, single use, non-toxic, non pyrogenic
2. The cannula with triple sharpening, it's polished, this makes
Injection painless.
3. The soft wings permit an easy grip making the fixing easy.
4. Colour codes to identify the diameter of the cannula (diameter of the
Cannula indicated on the wings)

Packing:
1. Polybag individual packing, 100PCS/box, 2000PCS/CTN
2. Blister packing, 100PCS/box, 2000PCS/CTN

infusion set component MOQ
with different model can be OEM requirement 100,000pcs
About us
Jiangsu Jichun Medical Devices Co., Ltd. was established in 1988 (with the original name Zhenglu Medical Materials Factory), is located in fertile Yangtze River Delta of Changzhou City, with the provincial road 232 passing by the gate of the company, with convenient transportation and advantageous environment. In 2008 in order to enlarge production scale, the company began land acquisition in Zhenglu industrial development zone and built the new plants, now covers a total area of 36, 000 square meters, with building area of 18, 000 square meters and class 100, 000 cleaning workshop area of 5, 500 square meters.
The company mainly deals with the development, production and marketing of the medical polymer medical devices for single use. The production capacity of the main products is: 1, 000 million sets of injection needles per year, 600 million sets of syringes per year and 100 million sets of infusion devices per year. The company is with beautiful surroundings, advanced equipments, well-equipped facilities, and all kinds of advanced product measuring instruments and scientific test methods. The 'Jichun' brand products produced in the company sell well worldwide, to Europe, America and Southeast Asia. Customers have high opinion of the quality and the service, with the cooperating partners and sales volum continuously increasing.increasing.
The company has a period of more than twenty years development history, with the distinctive human and geographic advantages that Changzhou is the old empire city and the location in Shanghai and Nanjing special economic zone, develops its own specialties in the aspects of injection molding, automatic assembly and packaging. The company has engaged senior top management, recruited lots of technicians, and established a complete set of quality management system. According to the requirements of ISO 13485: 2003/YY/T0287-2003 Medical devices_Quality management system_Requirements for Regulatory Purposes, Medical devices good manufacturing practice (try out), Medical devices good manufacturing practice Sterile medical devices implementation principles and inspection and evaluation standards (try out), US21 CFR Part 820 Medical devices current good manufacturing practice (cGMP), RDC59 Medical devices good manufacturing practice (GMP) and MDD 93/42/EEC Medical devices directive, assure the implementation and operation of the quality management system in the company.
In 2001 the company was appraised 'credible production of quality labeled enterprise' by Chinese Association for Medical Devices Industry, Chinese Nursing Association and Chinese Fundation for Customer Protection. In 2002 the company passed ISO9002 and CE Certification, and in 2004, passed the ISO9001/ISO13485 and CE Certification. We have pioneered a developing road dominant by the precise manufacture of medical devices for single use.single use.
In the new century, Jichun people will base on the market, look to the future, keep striving and forge ahead. We will seek the development of the company by the innovation of the concept, technology and system, to contribute to the human health.