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U.S. ATOMIC Form ANC-458 (4-4) ENERGY COMMISSION Form Approved Budget Bureau No. REGISTRATION CERTIFICATE-IN VITO TESTING WITH BYPRODUCT MATERIAL UNDER GENERAL LICENSE 10 CFR 31 38-R0160 Section 31.11

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What is registration certificate for in-vitro?

The registration certificate for in-vitro is a document that allows companies to legally market and sell in-vitro diagnostic medical devices.

Who is required to file registration certificate for in-vitro?

Companies manufacturing or distributing in-vitro diagnostic medical devices are required to file for a registration certificate.

How to fill out registration certificate for in-vitro?

The registration certificate for in-vitro can be filled out by providing all necessary information about the company and the in-vitro diagnostic medical devices being marketed.

What is the purpose of registration certificate for in-vitro?

The purpose of the registration certificate for in-vitro is to ensure that in-vitro diagnostic medical devices meet quality and safety standards before being marketed.

What information must be reported on registration certificate for in-vitro?

The registration certificate for in-vitro must include information about the company, in-vitro diagnostic devices being marketed, and compliance with regulations.

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