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Diasys Lipase Test (Non-Sterile) - Taiwan Registration 52f4916e0ff3c065fd6d620c2bdc3b60

Access comprehensive regulatory information for Diasys Lipase Test (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 52f4916e0ff3c065fd6d620c2bdc3b60 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT 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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52f4916e0ff3c065fd6d620c2bdc3b60
Registration Details
Taiwan FDA Registration: 52f4916e0ff3c065fd6d620c2bdc3b60
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Device Details

Diasys Lipase Test (Non-Sterile)
TW: ๅพท่ณฝ่„‚่‚ชๅˆ†่งฃ้…ต็ด ่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

52f4916e0ff3c065fd6d620c2bdc3b60

Ministry of Health Medical Device Import No. 021808

DHA09402180802

Company Information

Product Details

Limited to the first level identification range of the Lipolytic Enzyme Test System (A.1465) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1465 Lipolytic enzyme test system

Imported from abroad

Dates and Status

Jul 31, 2020

Jul 31, 2025