Taiwan FDA registration 6b8a1170997bc5a3ff23a0d2103532d3

“Haemonetics” High Efficiency Post-process Filter System for Leucocyte removal from red cells

TW: “漢尼帝克”白血球過濾套
Taiwan flagTaiwan·Risk Class 2·MD·Haemonetics Manufacturing, Inc.·Registered Dec 09, 2016 – Dec 09, 2026Active
Registration details
Analysis ID
6b8a1170997bc5a3ff23a0d2103532d3
License Form
Ministry of Health Medical Device Import No. 029160
Customs Code
DHA05602916006
Company information
Manufacturer Country
United States
Product details
Intended Use
This product is a container for the collection and processing of blood and blood components for the collection, storage or transportation of blood and its components for further processing.
Product Type (Level 1)
B Hematology and pathology devices
Product Type (Level 2)
B9100 Containers for the collection and processing of blood and blood components
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 09, 2016
Expiry Date
Dec 09, 2026
About this record

Access comprehensive regulatory information for “Haemonetics” High Efficiency Post-process Filter System for Leucocyte removal from red cells in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b8a1170997bc5a3ff23a0d2103532d3 and manufactured by Haemonetics Manufacturing, Inc.. The authorized representative in Taiwan is HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.).

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