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"DXN" a number of corrective products - Taiwan Registration 36d118de02201b54ac7bba07af13f118

Access comprehensive regulatory information for "DXN" a number of corrective products in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36d118de02201b54ac7bba07af13f118 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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36d118de02201b54ac7bba07af13f118
Registration Details
Taiwan FDA Registration: 36d118de02201b54ac7bba07af13f118
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Device Details

"DXN" a number of corrective products
TW: โ€œๅพทไฟกโ€ๅคš้ …ๆ กๆญฃๅ“
Risk Class 2

Registration Details

36d118de02201b54ac7bba07af13f118

DHA05603465300

Company Information

Product Details

Used in optical colorimetric analysis systems, it can be used for multiple quantitative corrections.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

Input;; QMS/QSD

Dates and Status

May 13, 2021

May 13, 2026