When medical device companies undergo FDA registration certification, they often encounter a term - "Dun & Bradstreet (D-U-N-S®) Number." Applying for a Dun & Bradstreet (D-U-N-S®) Number is a necessary prerequisite for companies to successfully complete FDA registration certification because it is required for establishing a company's paid account and applying for a UDI database account, among other steps. Today, JJRLAB is here to provide a detailed introduction to the Dun & Bradstreet (D-U-N-S®) Number.
The Dun & Bradstreet (D-U-N-S®) Number is a real-time dynamic enterprise identification consisting of 9 digits. It originates from the global coding system developed and managed by Dun & Bradstreet. It is widely used for enterprise identification, organization, and arrangement of business information, and can be used to identify and locate enterprise information quickly for risk management purposes.
As a globally recognized enterprise identification code, the Dun & Bradstreet (D-U-N-S®) Number is unique, with each enterprise entity having a corresponding code that is not reused, similar to an enterprise's ID number.
- When applying for a Dun & Bradstreet (D-U-N-S®) Number, companies need to submit information such as name and address. The FDA can identify and verify companies through the Dun & Bradstreet (D-U-N-S®) Number, which helps improve the quality and accuracy of FDA registration data.
- The Dun & Bradstreet (D-U-N-S®) Number is closely related to the credit evaluation of companies. The FDA can quickly and accurately check a company's history records, credit records, etc., through the Dun & Bradstreet (D-U-N-S®) Number to ensure the quality and safety of products.
- Company name in Chinese and English
- Company office address in Chinese and English
- Mailing address (if different from the office address, this information needs to be submitted)
- Name and position of company manager
- Number of employees
- Business contact person
- Phone number
- Position
- Type of business
- Scanned copy of business license
- Company authorization letter with seal and signature
JJRLAB is a "one-stop" medical device product quality service platform that integrates medical device product testing, certification, technical regulatory consultation, and clinical verification. With over twenty years of experience and technological innovation, JJRLAB has a technical team with both reputation and strength, capable of assisting medical device companies in quickly and accurately applying for a Dun & Bradstreet (D-U-N-S®) Number and providing them with one-stop medical device FDA registration certification services, helping companies smoothly enter the U.S. market.
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