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Abbott New Generation Hemolytic 1700 System - Taiwan Registration 25e8a6fa5af29318f21b9a5424a37eca

Access comprehensive regulatory information for Abbott New Generation Hemolytic 1700 System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 25e8a6fa5af29318f21b9a5424a37eca and manufactured by ABBOTT LABORATORIES. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC 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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25e8a6fa5af29318f21b9a5424a37eca
Registration Details
Taiwan FDA Registration: 25e8a6fa5af29318f21b9a5424a37eca
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Device Details

Abbott New Generation Hemolytic 1700 System
TW: ไบžๅŸนๆ–ฐไธ–ไปฃ่ก€็ƒๆบถ่งฃๅŠ‘1700็ณป็ตฑ
Risk Class 1
Cancelled

Registration Details

25e8a6fa5af29318f21b9a5424a37eca

DHA04400939601

Company Information

United States

Product Details

Limited to the first level identification range of red blood cell dissolving agent (B.8540) of the Measures for the Administration of Medical Devices.

B Hematology, pathology, and genetics

B.8540 ็ด…่ก€็ƒๆบถ่งฃๅŠ‘

import

Dates and Status

Oct 22, 2010

Oct 22, 2015

Aug 09, 2018

Cancellation Information

Logged out

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