Taiwan FDA registration 0cf824b280dd225c9af15fb1902cc0f8

Shengchuang blood component separator

TW: 笙創血液成份分離器

Taiwan·Risk Class 2·Shengchuang Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory·Registered Aug 30, 2011 – Aug 30, 2026Active

Registration details

Analysis ID: 0cf824b280dd225c9af15fb1902cc0f8
Customs Code: DHY00500339902

Company information

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

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
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: Contract manufacturing;; Domestic

Dates and status

Registration Date: Aug 30, 2011
Expiry Date: Aug 30, 2026

About this record

Access comprehensive regulatory information for Shengchuang blood component separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0cf824b280dd225c9af15fb1902cc0f8 and manufactured by Shengchuang Co., Ltd.;; Shengte Technology Co., Ltd. Yike Factory. 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.