Taiwan FDA registration e3282f3e79b49107108cab8937335f5d

"Shengchuang" Fenix Blood Fractionation Pack

TW: “笙創” 芬尼克斯血液分離組合包

Taiwan·Risk Class 2·Shengchuang Co., Ltd.; Shengte Technology Co., Ltd·Registered Dec 04, 2020 – Dec 04, 2025Expired

Registration details

Analysis ID: e3282f3e79b49107108cab8937335f5d

Company information

Manufacturer: Shengchuang Co., Ltd.; Shengte Technology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SAFETRAN BIOMEDICAL INC.

Product details

Intended Use: This product is used with the "Shengchuang" Fenix blood component separation equipment to provide the relevant consumables needed for the blood separation process.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9100 Containers for the collection and disposal of blood and blood components
Import Information: 國產;; QMS/QSD;; 委託製造

Dates and status

Registration Date: Dec 04, 2020
Expiry Date: Dec 04, 2025

About this record

Access comprehensive regulatory information for "Shengchuang" Fenix Blood Fractionation Pack in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3282f3e79b49107108cab8937335f5d and manufactured by Shengchuang Co., Ltd.; Shengte Technology Co., Ltd. The authorized representative in Taiwan is SAFETRAN BIOMEDICAL INC..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.