PMSSteripack Tyvek 灭菌包装袋(TP)和卷材(TY)带化学指示剂
K号: K160595 · 2016-11-18
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器械摘要
常见问题
What is the PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator?
PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator is a medical device that received FDA 510(k) clearance on 2016-11-18. The listed applicant is Pms Medikal Ambalaj Sanayi VE Ticaret Ltd Sti. The 510(k) number is K160595.
When did PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator receive FDA 510(k) clearance?
PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator received FDA 510(k) clearance on 2016-11-18, under 510(k) number K160595.
Who is the listed applicant for PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator?
The FDA 510(k) record lists Pms Medikal Ambalaj Sanayi VE Ticaret Ltd Sti as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator?
The FDA product code for PMSSteripack Tyvek Sterilization Pouch (TP) and Roll (TY) with Chemical Indicator is FRG.
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。
相关器械(代码:FRG)
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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