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Fadia Automation Instrument Series (Non-Sterile) - Taiwan Registration b5230e50216b7f656999cf5248662454

Access comprehensive regulatory information for Fadia Automation Instrument Series (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 b5230e50216b7f656999cf5248662454 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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b5230e50216b7f656999cf5248662454
Registration Details
Taiwan FDA Registration: b5230e50216b7f656999cf5248662454
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Device Details

Fadia Automation Instrument Series (Non-Sterile)
TW: ๆณ•่ฟชไบž ่‡ชๅ‹•ๅŒ–ๅ„€ๅ™จ็ณปๅˆ— (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

b5230e50216b7f656999cf5248662454

DHA084A0034202

Company Information

Sweden

Product Details

It is limited to the first level of identification of the classification and grading management of medical devices "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)".

A Clinical chemistry and clinical toxicology

A.2160 Individual Photometric Chemistry Analyzer for Clinical Use

import

Dates and Status

Dec 24, 2024

Oct 31, 2026