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Fuji Ammonia Analyzer (Unsterilized) - Taiwan Registration b66e9e4da4428bd3e108403d1e00ad72

Access comprehensive regulatory information for Fuji Ammonia Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b66e9e4da4428bd3e108403d1e00ad72 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is HUNG CHONG CORP..

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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b66e9e4da4428bd3e108403d1e00ad72
Registration Details
Taiwan FDA Registration: b66e9e4da4428bd3e108403d1e00ad72
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Device Details

Fuji Ammonia Analyzer (Unsterilized)
TW: ๅฏŒๅฃซ่ก€ๆฐจๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b66e9e4da4428bd3e108403d1e00ad72

DHA04400838807

Company Information

Product Details

Limited to the first level identification range of the blood ammonia test system (A.1065) of the management method for medical equipment.

A Clinical chemistry and clinical toxicology

A.1065 ่ก€ๆฐจ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Dec 15, 2009

Dec 15, 2014

Apr 25, 2018

Cancellation Information

Logged out

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