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"Hannitec" automatic blood separator - Taiwan Registration 2ae46a233d198931d5177d31f7120333

Access comprehensive regulatory information for "Hannitec" automatic blood separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2ae46a233d198931d5177d31f7120333 and manufactured by HAEMONETICS CORPORATION. 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.

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2ae46a233d198931d5177d31f7120333
Registration Details
Taiwan FDA Registration: 2ae46a233d198931d5177d31f7120333
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Device Details

"Hannitec" automatic blood separator
TW: โ€œๆผขๅฐผๅธๅ…‹โ€่‡ชๅ‹•่ก€ๆถฒๅˆ†้›ขๆฉŸ
Risk Class 3
Cancelled

Registration Details

2ae46a233d198931d5177d31f7120333

DHA00601931102

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

B Hematology, pathology, and genetics

B.9245 Automated hemocytoseparator

import

Dates and Status

Oct 30, 2008

Oct 30, 2018

Jun 16, 2022

Cancellation Information

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