3 Part Medical Plastic Disposable Syringe with Needle

3 Part Medical Plastic Disposable Syringe with Needle

3部件医用塑料一次性注射器带针

3000000+
0.02 USD

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型号。 1mL,2mL(2.5mL),3mL,5mL,10mL,20mL,30mL,50mL,
材料 塑料
应用
证明 ce,sgs,iso13485
用针
消毒 消毒
医疗器械注册/记录号 Gxxz20153151378
证书 ce,iso,gmp
商标 jmd或oem
规范 1,2,3,5,10,12,20,30,50,60,100ml
HS编码 90183100
类型 注射器
1,2,3,5,10,20,30,50,100ml
特征 一次性
成人
注射器使用 肌内注射
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,或散装
起源 中国常州
3部分医用塑料一次性注射器带针
注射器类型 3部分路厄可滑动注射器
材料 塑料
1mL,2mL(2.5mL),3mL,5mL,10mL,20mL,30mL,50mL,60mL。
应用
特征 一次性
证明 ce,sgs,iso13485,
15G-30G,带针和无针
注射器使用 静脉注射
吸塑或PE包装
Specificaition iso,ce,gmp
样品 自由
交货日 20天
喷嘴 中央喷嘴或侧喷嘴
柱塞类型 透明,白色,蓝色
透明
无菌 通过EO气体无菌,无毒,无热原



特征:
一次性注射器,用于皮下注射,肌内注射和静脉注射。
1.通过EO气体灭菌,无毒,无致热,仅一次使用。
Luer Slip或Luer Lock。
3.足够透明的桶容易测量注射器中容纳的体积和气泡的检测。
桶上刻度刻度很容易阅读。毕业印刷由不可磨灭的墨水。
柱塞非常适合于柱塞内部,以便自由平稳运动。
桶和柱塞材料:医用级PP(聚丙烯)。
7.垫片材质:天然胶乳/合成橡胶(无胶乳)。
有或没有针。
9.个人包装:吸塑包/袋子。
10.可用尺寸:1mL,2mL(2.5mL),3mL,5mL,10mL,20mL,30mL,50mL,60mL。
11.标准:ISO7886-1:1993。
尺寸 包装 用针或无针 鲁尔或鲁尔锁
1毫升 PE或吸塑
2毫升 PE或吸塑
3毫升 PE或吸塑
5毫升 PE或吸塑
10毫升 PE或吸塑
20毫升 PE或吸塑
30毫升 PE或吸塑
50毫升 PE或吸塑
60毫升 PE或吸塑
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. 1mL, 2mL(2.5mL), 3mL, 5mL, 10mL, 20mL, 30mL, 50mL,
Material Plastic
Application Medical
Certification CE, SGS, ISO13485
Needle With Needle
Disinfection Disinfection
Medical Devices Reg./Record No. Gxxz20153151378
Certificates CE, ISO, GMP
Trademark JMD or OEM
Specification 1, 2, 3, 5, 10, 12, 20, 30, 50, 60, 100ML
HS Code 90183100
Type Syringe
Volume 1,2,3,5,10,20,30,50,100ml
Feature Disposable
Group Adult
Syringe Use Intramuscular Injection
Medical Device Regulatory Type Type 3
Brand Jmd or OEM
ISO Certificate ISO13485, ISO9001
Transport Package PE or Blister, or Bulk
Origin Changzhou, China
3 Part Medical Plastic Disposable Syringe with Needle
Syringe Type 3 part luer slip dispodable syringe
Material Plastic
Volume 1mL, 2mL(2.5mL), 3mL, 5mL, 10mL, 20mL, 30mL, 50mL, 60mL.
Application Medical
Feature Disposable
Certification CE, SGS , ISO13485,
needle 15G-30G , with and without needle
Syringe Use Instranuscular Injection
Package Blister or PE packing
Specificaition ISO, CE, GMP
Sample Free
Delivery days 20days
Nozzle Central nozzel or side nozzle
Plunger type Transparent , white , blue
Barrel Transparent
Sterile sterile by EO gas , non-toxic , non-pyrogen



Feature:
Disposable syringe for hypodermic, intramuscular and intravenous injection.
1. Sterilized by EO gas, non-toxic, non-pyrogenic, single use only.
2. Luer Slip or Luer Lock.
3. Sufficiently transparent barrel allows easy measurement of the volume contained in the syringe and detection of air bubble.
4. Graduated scale on the barrel is easy to read. Graduation is printed by indelible ink.
5. The plunger fits the inside of barrel very well to allow for free and smooth movement.
6. Material for barrel and plunger: Medical grade PP(polypropylene).
7. Material for gasket: Natural latex / Synthetic rubber(latex free).
8. With or without needle.
9. Individual pack: Blister pack / Polybag.
10. Available size: 1mL, 2mL(2.5mL), 3mL, 5mL, 10mL, 20mL, 30mL, 50mL, 60mL.
11. Standard: ISO7886-1: 1993.
size packing with needle or without needle luer slip or luer lock
1ml PE or Blister both both
2ml PE or Blister both both
3ml PE or Blister both both
5ml PE or Blister both both
10ml PE or Blister both both
20ml PE or Blister both both
30ml PE or Blister both both
50ml PE or Blister both both
60ml PE or Blister both both
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.