免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

德文 blastocyst 中間培養基(含HSA與不含HSA)

K 號:K231370 · 2023-08-04

決定日期2023-08-04
產品代碼MQL
諮詢委員會OB設備之醫療設備規範文本翻譯如下: 關於OB設備的醫療設備規範文件: 此設備已通過FDA認證,並獲得510(k)許可證。該設備的PMA申請已提交,並在NCT登錄編號為[編號]的研究中進行測試。相關文獻的PMID編號為[編號]。請參考以下識別碼和網址: 識別碼:[識別碼] 網址:[網址] 政策:醫療規範-v1
決定相當於

器材摘要

Dewin Blastocyst Medium (with HSA and without HSA) is the device name listed in this FDA 510(k) record. The listed applicant is Donnevie Medical Technology (Shanghai) Co. , Ltd.. It received FDA 510(k) clearance on 2023-08-04 under 510(k) number K231370. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Dewin Blastocyst Medium (with HSA and without HSA)?

Dewin Blastocyst Medium (with HSA and without HSA) is a medical device that received FDA 510(k) clearance on 2023-08-04. The listed applicant is Donnevie Medical Technology (Shanghai) Co. , Ltd.. The 510(k) number is K231370.

When did Dewin Blastocyst Medium (with HSA and without HSA) receive FDA 510(k) clearance?

Dewin Blastocyst Medium (with HSA and without HSA) received FDA 510(k) clearance on 2023-08-04, under 510(k) number K231370.

Who is the listed applicant for Dewin Blastocyst Medium (with HSA and without HSA)?

The FDA 510(k) record lists Donnevie Medical Technology (Shanghai) Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dewin Blastocyst Medium (with HSA and without HSA)?

The FDA product code for Dewin Blastocyst Medium (with HSA and without HSA) is MQL.

相關臨床試驗

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

其他以 Donnevie Medical Technology (Shanghai) Co. , Ltd. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

相關器械(代碼:MQL)

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係,請查閱連結的官方來源。

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。

↑