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Analyticon combi scan 500 (Non-Sterile) - Taiwan Registration 10d61f9824a132063213d0ed090c1af0

Access comprehensive regulatory information for Analyticon combi scan 500 (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 10d61f9824a132063213d0ed090c1af0 and manufactured by ANALYTICON BIOTECHNOLOGIES AG. The authorized representative in Taiwan is IN FUNG CO., LTD..

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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10d61f9824a132063213d0ed090c1af0
Registration Details
Taiwan FDA Registration: 10d61f9824a132063213d0ed090c1af0
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Device Details

Analyticon combi scan 500 (Non-Sterile)
TW: ๅบทๆฏ”ๅฐฟๆถฒ็”ŸๅŒ–ๆชขๆธฌ่ฉฆ็ด™ๅˆค่ฎ€ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

10d61f9824a132063213d0ed090c1af0

Ministry of Health Medical Device Import Registration No. 002271

DHA08400227105

Company Information

Product Details

Automatic interpretation of urine test strips

A Clinical chemistry and clinical toxicology

A2900 Automated Urinalysis System

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026