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Combi Screen XL (Non-Sterile) - Taiwan Registration 433da75e2747be66dd9e2f0070f711c1

Access comprehensive regulatory information for Combi Screen XL (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 433da75e2747be66dd9e2f0070f711c1 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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433da75e2747be66dd9e2f0070f711c1
Registration Details
Taiwan FDA Registration: 433da75e2747be66dd9e2f0070f711c1
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Device Details

Combi Screen XL (Non-Sterile)
TW: ๅบทๆฏ”่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

433da75e2747be66dd9e2f0070f711c1

Ministry of Health Medical Device Import Registration No. 006381

DHA08400638106

Company Information

Product Details

Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A2900 Automated Urinalysis System

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023