| 营业 | 周6、日、节日休息 |
|---|---|
| 上班 | 9-17（24小时制） |
| 电话 | 8613685252668 8613685252668 ☎ |
| 地址 | Zhenglu Industrial Park, Wujin, Changzhou, Jiangsu, China 213111（请用顶部导航） |
| 联系 | Ms. Kathy |
江苏吉春医疗器械有限公司成立于1988年（原名为正禄医用材料厂），位于常州市长江三角洲，省道232路经公司门口，方便交通和有利环境。 2008年为了扩大生产规模，公司开始在郑路工业开发区征地，建设新厂房，现占地面积36万平方米，建筑面积18万平方米，100级， 000清洗车间面积为5,500平方米。
公司主要从事医疗高分子医疗器械的开发，生产和销售。主要产品的生产能力为：每年注射针头1000万套，每年注射器6亿套，每年输注器械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”品牌产品销往世界各地，欧洲，美洲和东南亚。客户对质量和服务有着高度的评价，与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，具有独特的人文和地理优势，常州是老帝国城市，位于上海和南京特色经济区，在注塑，自动化装配和包装。公司聘请了高级管理人员，招聘了大批技术人员，建立了一套完整的质量管理体系。根据ISO 13485：2003 / YY / T0287-2003的要求医疗器械 - 质量管理体系 - 管理目的的要求，医疗器械良好的制造实践（试验），医疗器械良好的制造实践无菌医疗器械实施原则和检查和评估标准出口），US21 CFR第820部分医疗器械现行良好生产规范（cGMP），RDC59医疗器械良好生产规范（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护基金会评为“可靠生产优质贴标企业”。 2002年公司通过ISO9002和CE认证，并于2004年通过了ISO9001 / ISO13485和CE认证。我们通过精确制造一次性使用的医疗器械，率先开发了一条发展中的道路。
在新世纪，吉春人将立足市场，展望未来，不断努力奋进。我们将通过创新的理念，技术和系统，寻求公司的发展，为人类健康做出贡献。
公司主要从事医疗高分子医疗器械的开发，生产和销售。主要产品的生产能力为：每年注射针头1000万套，每年注射器6亿套，每年输注器械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”品牌产品销往世界各地，欧洲，美洲和东南亚。客户对质量和服务有着高度的评价，与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，具有独特的人文和地理优势，常州是老帝国城市，位于上海和南京特色经济区，在注塑，自动化装配和包装。公司聘请了高级管理人员，招聘了大批技术人员，建立了一套完整的质量管理体系。根据ISO 13485：2003 / YY / T0287-2003的要求医疗器械 - 质量管理体系 - 管理目的的要求，医疗器械良好的制造实践（试验），医疗器械良好的制造实践无菌医疗器械实施原则和检查和评估标准出口），US21 CFR第820部分医疗器械现行良好生产规范（cGMP），RDC59医疗器械良好生产规范（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护基金会评为“可靠生产优质贴标企业”。 2002年公司通过ISO9002和CE认证，并于2004年通过了ISO9001 / ISO13485和CE认证。我们通过精确制造一次性使用的医疗器械，率先开发了一条发展中的道路。
在新世纪，吉春人将立足市场，展望未来，不断努力奋进。我们将通过创新的理念，技术和系统，寻求公司的发展，为人类健康做出贡献。
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.
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.
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.
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.
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.
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.