the 510(k) Submission
更新:2023-12-21 16:36 编号:26253581 发布IP:112.112.120.160 浏览:9次- 发布企业
- 上海角宿企业管理咨询有限公司商铺
- 认证
- 资质核验:已通过营业执照认证入驻顺企:第6年主体名称:上海角宿企业管理咨询有限公司组织机构代码:91310115MA1HA14X7W
- 报价
- 人民币¥18000.00元每件
- 美国FDA
- 授权代表
- 可加急
- 简化提交流程
- 国内外
- 顺利注册
- 关键词
- FDA510k
- 所在地
- 中国(上海)自由贸易试验区临港新片区宏祥北路83弄1-42号20幢118室(注册地址)
- 联系电话
- 021-20960309
- 手机
- 18717927910
- 联系人
- Cabebe 请说明来自顺企网,优惠更多
详细介绍
YourGateway to the U.S. Medical Device Market-- the 510(k)Submission
For medical device manufacturers aiming toenter the U.S. market, the 510(k) submission process is a pivotalstep. Understanding and mastering this process is synonymous withunlocking the potential to reach the largest healthcare market inthe world.
The Essence of 510(k) SubmissionServices:
The 510(k) submission, also known as aPre-market Notification, is a regulatory filing that demonstratesto the U.S. Food and Drug Administration (FDA) that your medicaldevice is substantially equivalent to a device that is alreadylegally marketed. The intricacy of this process necessitates acomprehensive, detailed, and efficient submission packet tovalidate the safety and effectiveness of your product.
Why Opt for Professional 510(k) Submission Services?
Expertise: Service providers with expertisein FDA communications possess the skills to identify optimalpredicate devices and craft persuasive substantial equivalencearguments.
Time Efficiency: Staying abreast of theFDA’s current requirements and guidance can help you avoidunnecessary setbacks and expedite market entry.
Risk Reduction: Professional 510(k)submission services minimize the errors that can occur during thesubmission process, reducing the risk of denial.
Customization: Every medical device projectis unique; professional submission services offer tailoredsolutions to meet your specific needs.
How Can 510(k) Submission Services AssistYou?
Our service teams support you in organizing and preparingFDA-compliant documentation and also provide strategic planning,risk assessment, and pre-submission consulting. Our aim is tocreate a smooth pathway for your product from the laboratory to themarket.
Conclusion:
Whether you are a start-up or an industrytitan, professional FDA 510(k) submission services are key toensuring that your medical device successfully penetrates the U.S.market. Choose the right partner to take your product from thebench to the bedside, opening a new chapter in your businessgrowth.
法定代表人 | 张陈燕 | ||
注册资本 | 200万人民币 | ||
主营产品 | FDA注册,510K,美国代理人,验厂;CE, 欧代,欧洲自由销售证书CFS,MHRA注册,UKCA;TGA注册;ISO13485质量管理体系;海牙/使馆认证... | ||
经营范围 | 企业管理咨询,商务信息咨询。【依法须经批准的项目,经相关部门批准后方可开展经营活动】 | ||
公司简介 | 上海角宿企业管理咨询有限公司创建于2018年,是全球医疗器械法规第三方咨询服务提供者。主营业务有:FDA注册,510K,美国代理人,验厂;CE,欧代,欧洲自由销售证书,MHRA注册,UKCA;TGA注册;ISO13485质量管理体系;海牙/使馆认证等,角宿还为医疗器械产业良好经营规范提供技术指导、医疗器械产品市场准入合规评估、全球主要市场监管机构注册、国内厂商出口许可、海外代理人等综合性咨询服务。 ... |
- 解读FDA新规:AI医疗器械变革之路一、FDA新规重磅来袭近期,美国食品药品监督管理局(FDA)发布了一则在医疗器械... 2025-01-15
- 加拿大医疗器械MDEL许可证:更新注册全解析一、引言在加拿大从事医疗器械行业,MDEL许可证是极为关键的“入场券”。它关乎企... 2025-01-14
- 食品 FDA 注册认证的具体要求什么是FDA注册认证美国食品药品监督管理局(FDA),作为美国卫生与公众服务部的... 2025-01-13
- 咖啡出口美国,FDA 注册很关键!咖啡,作为世界三大饮料之一,早已融入美国民众的日常生活。据统计,超一亿美国成年人... 2025-01-10
- 精油出口沙特,SFDA 注册全攻略沙特精油市场潜力剖析沙特阿拉伯,作为中东地区的关键经济体,近年来其美容与个人护理... 2025-01-09
- 医疗器械认证指导--二类医疗器械申请CE认证好文19,990.00元/件
欧盟CE:授权代表 - 医疗器械注册导航--牙齿保持器申请沙特SFDA认证指导20,000.00元/件
SFDA:授权代表 - 合规咨询:儿童退热贴在国内注册指导18,000.00元/件
中国药监局:授权代表 - ISO 13485:2016和GMP的主要差异和不同之处是什么?20,000.00元/件
ISO:授权代表 - ISO 13485:2016和GMP的共同点和相似之处是什么?20,000.00元/件
ISO:授权代表 - 哪些产品受FDA管控?20,000.00元/件
美国FDA:授权代表 - 欧盟进口商的责任是什么?20,000.00元/件
欧盟CE:授权代表 - MDR中警戒系统的重要性介绍20,000.00元/件
MDR:授权代表 - 欧盟制造商在危机管理中的职责是什么?20,000.00元/件
欧盟CE:授权代表 - 揭秘欧盟医疗器械法规的危机管理的定义与原则20,000.00元/件
欧盟CE:授权代表