Taiwan FDA registration 8ee5658d027f79373550f6122a069408

"Hannitec" de-leukocyte platelet processing filter

TW: “漢尼帝克”去白血球血小板處理過濾器

Taiwan·Risk Class 2·Haemonetics Manufacturing, Inc.;; Haemonetics Corporation·Registered Aug 02, 2011 – Aug 02, 2026Active

Registration details

Analysis ID: 8ee5658d027f79373550f6122a069408
Customs Code: DHA00602266001

Company information

Manufacturer: Haemonetics Manufacturing, Inc.;; Haemonetics Corporation
Manufacturer Country: United States
Authorized Representative: HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.)

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5440 血管內輸液套
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Aug 02, 2011
Expiry Date: Aug 02, 2026

About this record

Access comprehensive regulatory information for "Hannitec" de-leukocyte platelet processing filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8ee5658d027f79373550f6122a069408 and manufactured by Haemonetics Manufacturing, Inc.;; Haemonetics Corporation. The authorized representative in Taiwan is HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.).

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