Taiwan FDA registration 41f28c7718710dacc130ad98dde9a56a

Anfutri high-concentration platelet plasma separation tube

TW: 安福萃高濃度血小板血漿分離管

Taiwan·Risk Class 2·Rmedica Co., Ltd·Registered Dec 02, 2019 – Dec 02, 2029Active

Registration details

Analysis ID: 41f28c7718710dacc130ad98dde9a56a
Customs Code: DHA05603309500

Company information

Manufacturer: Rmedica Co., Ltd
Manufacturer Country: Korea, Republic of
Authorized Representative: Zhiding Biotechnology CO., LTD.

Product details

Intended Use: This product collects a small amount of patient blood and prepares autologous platelet thick fluid.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9245 Automated hemocytoseparator
Import Information: import

Dates and status

Registration Date: Dec 02, 2019
Expiry Date: Dec 02, 2029

About this record

Access comprehensive regulatory information for Anfutri high-concentration platelet plasma separation tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41f28c7718710dacc130ad98dde9a56a and manufactured by Rmedica Co., Ltd. The authorized representative in Taiwan is Zhiding Biotechnology CO., LTD..

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