Taiwan FDA registration d20fddb06674f9b0ea8de75d43d55631

"Hannitic" removes the white blood cell filter

TW: “漢尼帝克”去除白血球過濾器

Taiwan·Risk Class 2·Haemonetics Manufacturing, Inc.;; Haemonetics Corporation·Registered Sep 19, 2011 – Sep 19, 2026Active

Registration details

Analysis ID: d20fddb06674f9b0ea8de75d43d55631
Customs Code: DHA00602281106

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: import

Dates and status

Registration Date: Sep 19, 2011
Expiry Date: Sep 19, 2026

About this record

Access comprehensive regulatory information for "Hannitic" removes the white blood cell filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d20fddb06674f9b0ea8de75d43d55631 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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