USFDA 医疗器械法规简介

22 4 月, 2025 by mambani

Join Registrar Corp’s experts as they break down the fundamentals of medical device regulation in the United States. From device classification and 510(k) requirements to registration, labeling, and UDI compliance, this session is ideal for medical device companies looking to enter or expand in the U.S. market.

加入 Registrar Corp 的专家，他们将分解美国医疗器械监管的基本知识。从设备分类和 510（k） 要求到注册、标签和 UDI 合规性，本次会议是希望进入或扩展美国市场的医疗设备公司的理想选择。

Don’t wait! Renew your
FDA registration today.

Registrar Corp will help you re-register with FDA quickly and properly.

For more assistance with FDA regulatory requirements, call: +1-757-224-0177, email: info@registrarcorp.com, or chat with a Regulatory Advisor 24-hours a day: www.registrarcorp.com/livechat.

Get Assistance Today
single-box-image

Subscribe To Our News Feed

To top
This site is registered on wpml.org as a development site. Switch to a production site key to remove this banner.