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Multiple Blood Component Collection System "Hannitec" - Taiwan Registration 0b84377ac083c3e059b81e0e5f73ace0

Access comprehensive regulatory information for Multiple Blood Component Collection System "Hannitec" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b84377ac083c3e059b81e0e5f73ace0 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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0b84377ac083c3e059b81e0e5f73ace0
Registration Details
Taiwan FDA Registration: 0b84377ac083c3e059b81e0e5f73ace0
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Device Details

Multiple Blood Component Collection System "Hannitec"
TW: ๅคš้‡่ก€ๆถฒๆˆๅˆ†ๆ”ถ้›†็ณป็ตฑใ€€ใ€ๆผขๅฐผๅธๅ…‹ใ€ž
Risk Class 2
Cancelled

Registration Details

0b84377ac083c3e059b81e0e5f73ace0

DHA00600850402

Company Information

United States

Product Details

0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment

import

Dates and Status

Dec 22, 1997

Feb 09, 2019

Jun 16, 2022

Cancellation Information

Logged out

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