Taiwan FDA registration fb6af4167c473e49df082271cdfeff0d

"Hannitec" single-use platelet white blood cells filter blood bags

TW: “漢尼帝克”一次性使用血小板型白血球過濾血袋

Taiwan·Risk Class 2·Haemonetics Manufacturing, Inc.·Registered Oct 30, 2012 – Oct 30, 2022Cancelled

Registration details

Analysis ID: fb6af4167c473e49df082271cdfeff0d
Customs Code: DHA00602414709

Company information

Manufacturer: Haemonetics Manufacturing, Inc.
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): B Hematology, pathology, and genetics
Product Type (Level 2): B.9100 Containers for the collection and disposal of blood and blood components
Import Information: import

Dates and status

Registration Date: Oct 30, 2012
Expiry Date: Oct 30, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Hannitec" single-use platelet white blood cells filter blood bags in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb6af4167c473e49df082271cdfeff0d and manufactured by Haemonetics Manufacturing, Inc.. The authorized representative in Taiwan is HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.).

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.