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丹麥能肯(Nunc)     
丹麥NUNC能肯 ：丹麥NUNC公司自1953年起致力于生命科學領域，以生產(chǎn)高品質(zhì)的塑料制品而蜚聲于生物制藥和生命科學領域。今天，NUNC公司仍然位于整個生命科學市場的前列，并且持續(xù)發(fā)展創(chuàng)新的核心技術，以保證在未來變幻的市場中能夠保持成功。在生產(chǎn)領域中，NUNC公司是取得了ISO9001：2000認證，提供了應用于細胞培養(yǎng)、分子生物學、染色體和免疫學中的實驗室塑料制品。Nunc產(chǎn)品包括：細胞培養(yǎng)、生物制備、免疫化驗、分子生物、微陣列產(chǎn)品、臨床微生物、凍存系列產(chǎn)品、液體儲存和處理、液體操作系列等。
賽默飛世爾科技（Thermo Fisher Scientific（紐約證交所代碼：TMO），原美國熱電公司）實驗室消耗品部（LCD）為用戶提供世界一流的實驗室消耗品，主要包括移液器，實驗室塑料制品和實驗室玻璃器皿三大類產(chǎn)品。旗下?lián)碛斜姸嘀a(chǎn)品線：Thermo Scientific Finnpipette，MBP/QSP，NALGENE，NUNC，Matrix等。
 
Nunc is part of Thermo Fisher Scientific and an internationally known and well-established (since 1953) brand of high tech disposable plastic ware fulfilling the needs of today’s customers within biotechnology, pharmaceutical and research laboratories as well as in the production of vaccines and diagnostic kits.

Nunc brand is committed to playing an important role in the development of new products and surface treatments which will help scientists to produce results and to find industrial applications for discoveries made in pure science.

Nunc is Latin for “NOW” and as such Nunc’s name is synonymous with innovation. Coupled with cooperation, quality and service we have made this our aim.

Customisation matching your needs
If you do not find what you need in our catalogue or the web site please ask. In many cases we may be able to provide what you need as a customised product, just for you.

Technical service
We also help our customers use our products to their best advantage. As a Nunc customer you have the expertise of our R&D staff at your disposal if you have application enquiries. When you contact us, you can expect advice on product choice and all aspects of the application of our products.

Quality
Quality involves all aspects of our organisation from product development, choice of raw materials, through production to customer service. It is no accident that our quality control and assurance department is the largest in the company. Nunc is certified to ISO 9001:2000 and ISO 13485:2003 and designed to comply with US current Good Manufacturing Practice for Medical Devices.