China Diabetes Adjustable Blood Lancing Device With Lancet Eject - China
price: contact company for price
1 - Material: Spring and PE 2 - Product Use: It can be used to clinical blood testing and diabetes self-test use with lancet 3 - Specification: 5 depth levels 4 - Color: White, Gray 5 - Product characteristics : This kind lancing device assist diabete patients to monitor their glucose levels, easily and safely with an adjustable dial;Lancing depth can be set to an appropriate level for the individual;
More safe professional system that the lancing devices with ejector for the lancets disposal;
Any standard lancet can be used with these devices.
6 - ISO13485 ISO9001 CE0123 FDA
Company Contact:
- Phone: 86-0531-61328777
- Address: No.1,Shuangshan Sanjian Road, Jinan , Shandong , China
- Email:
Published date: June 4, 2018
- Business Description: Contact person: Mr.
Shen
Phone: +86-15689695066
Em ail: jane@lianyingchina.
com
Sk ype : Henry0871
Whats app: 8615098983602
Website: http: //www.
sdlianfa.
com/index.
php?lang=en
Company Description: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD
Shandong Lianfa Medical Plastic Products Co., Ltd. is a standard joint-venture enterprise incorporated with AMAX Group of America.
It established in 1992 .
The company is located at the beautiful east city industrial zone , zhangqiu City, jinan .
The total area is 20, 000 square meters, including a 100 thousand GMP cleanroom which is 8, 000 square meters and a 10 thousand cleanroom which is 2, 000 square meters .
The advanced lab system include a biological lab, a chemical lab, a physical lab, a measuring room and an observing animal room.
Green area reaches more than 50% .
Mainly products are medical devices which including Comfort Lancet , Lancing Device, Safety Lancet,
Heel Blade Safety Lancet , which are exported to the United States, Brazil, Canada, Europe and other
countries and regions, we have cooperated with many famous international glucose meter manufacturers.
We have obtained the ISO9001 in 1998, ISO13485 and CE registration in 2003 , FDA registration in 2005 and UL audit of America.
We also pass the Korea audit in 2016.
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