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NRC Form 483 (1281) 10 CFR 31U. S. NUCLEAR REGULATORY COMMISSIONREGISTRATION CERTIFICATE IN VITO TESTING WITH BYPRODUCT MATERIAL UNDER GENERAL LICENSEApproved t Dy OMB 31500 035 1314 34Section 31.11

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Who needs registration certificate for in-vitro?

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Anyone involved in conducting in-vitro fertilization procedures, such as fertility clinics, medical facilities, or research institutions, may need a registration certificate for in-vitro.

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What is registration certificate for in-vitro?

The registration certificate for in-vitro is a document that authorizes the use of in-vitro diagnostic medical devices.

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

Manufacturers and importers of in-vitro diagnostic medical devices are required to file the registration certificate.

How to fill out registration certificate for in-vitro?

The registration certificate for in-vitro can be filled out online on the designated government website.

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

The purpose of the registration certificate is to ensure the safety and efficacy of in-vitro diagnostic medical devices.

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

Information such as device name, manufacturer details, intended use, and risk classification must be reported on the registration certificate.

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