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WINNOMED COMPANY LTD.

Certification

  • Taiwantrade Advanced Verified

    Advanced check: The company's legal existence is checked against a government database. The company's operating status is third-party verified by Dun & Bradstreet/TÜV Rheinland.

  • The D&B D-U-N-S® Number is D&B's distinctive nine-digit identification sequence, which links you to a wealth of quality information products and services originating exclusively from D&B. The D&B D-U-N-S® Number is an internationally recognized common company identifier in EDI and global electronic commerce transactions.

The world's most influential standards-setting organizations, more than 50 global, industry and trade associations, and the U.S. Federal Government recognize, recommend and/or require the D&B D-U-N-S® Number.

D&B D-U-N-S® Numbers are the key to building corporate family relationships in the D&B file. Since each location of a business may have its own unique D&B D-U-N-S® Number, a large organization is likely to have many different D&B D-U-N-S® Numbers within its corporate "family." D&B links the D&B D-U-N-S® Numbers of parents, subsidiaries, headquarters and branches on more than 70 million corporate family members around the world.

    The D&B D-U-N-S® Number is D&B's distinctive nine-digit identification sequence, which links you to a wealth of quality information products and services originating exclusively from D&B. The D&B D-U-N-S® Number is an internationally recognized common company identifier in EDI and global electronic commerce transactions. The world's most influential standards-setting organizations, more than 50 global, industry and trade associations, and the U.S. Federal Government recognize, recommend and/or require the D&B D-U-N-S® Number. D&B D-U-N-S® Numbers are the key to building corporate family relationships in the D&B file. Since each location of a business may have its own unique D&B D-U-N-S® Number, a large organization is likely to have many different D&B D-U-N-S® Numbers within its corporate "family." D&B links the D&B D-U-N-S® Numbers of parents, subsidiaries, headquarters and branches on more than 70 million corporate family members around the world.

  • The verification certificate for TAITRA aims to ensure the qualification of a supplier who is going to join Taiwantrade e-commerce platform. Business information such as company name/address, email address, company ID, telephone number, employee number, revenue, main product, management personnel, etc. will be verified by TUV Rheinland Taiwan to guarantee the authenticity. After that, verification certificate and test mark will be issued with validity of one year.

Product Certification (3)

  • CE Marking (EU Standards)
The safety mark is a mandatory conformity mark on designated products placed on the single market in the European Union (EU).
This mark is possible to be affixed to only the products that conform to the safety regulation, that the directives
from the ministerial conference of the European Communities show.
  • The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human Services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed[5] and veterinary products.

The FDA was empowered by the United States Congress to enforce the Federal Food, Drug, and Cosmetic Act, which serves as the primary focus for the Agency; the FDA also enforces other laws, notably Section 361 of the Public Health Service Act and associated regulations, many of which are not directly related to food or drugs. These include regulating lasers, cellular phones, condoms and control of disease on products ranging from certain household pets to sperm donation for assisted reproduction.
  • ISO 13485:2016 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). ISO 13485:2016 can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.