Dynax 清晰型，Dynax 腊状，Dynax 重型，Dynax 轻型，Dynax 单一型
K号: K171562 · 2018-04-13
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器械摘要
常见问题
What is the Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono?
Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono is a medical device that received FDA 510(k) clearance on 2018-04-13. The listed applicant is Dreve Dentamid GmbH. The 510(k) number is K171562.
When did Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono receive FDA 510(k) clearance?
Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono received FDA 510(k) clearance on 2018-04-13, under 510(k) number K171562.
Who is the listed applicant for Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono?
The FDA 510(k) record lists Dreve Dentamid GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono?
The FDA product code for Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono is ELW.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
列明Dreve Dentamid GmbH为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：ELW）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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