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Phadia System (Non-Sterile) - Taiwan Registration fe98d7cc5edb1dff18406921ed465221

Access comprehensive regulatory information for Phadia System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fe98d7cc5edb1dff18406921ed465221 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..

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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fe98d7cc5edb1dff18406921ed465221
Registration Details
Taiwan FDA Registration: fe98d7cc5edb1dff18406921ed465221
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Device Details

Phadia System (Non-Sterile)
TW: ๆณ•่ฟชไบž(่‡ชๅ‹•ๅŒ–ๅ„€ๅ™จ)็ณปๅˆ—(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

fe98d7cc5edb1dff18406921ed465221

Ministry of Health Medical Device Import Registration No. 005250

DHA08400525002

Company Information

Sweden

Product Details

Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A2160 Individual photometric chemistry analyzer for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026