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Wei Di Automatic Urine Analyzer (Unsterilized) - Taiwan Registration 588c641b6dbe4c540de265dbd5687db9

Access comprehensive regulatory information for Wei Di Automatic Urine Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 588c641b6dbe4c540de265dbd5687db9 and manufactured by YD DIAGNOSTICS CORPORATION. The authorized representative in Taiwan is TUNYEN TECHNOLOGY 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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588c641b6dbe4c540de265dbd5687db9
Registration Details
Taiwan FDA Registration: 588c641b6dbe4c540de265dbd5687db9
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Device Details

Wei Di Automatic Urine Analyzer (Unsterilized)
TW: ๅ‰ๅปธ่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

588c641b6dbe4c540de265dbd5687db9

DHA04400662702

Company Information

Korea, Republic of

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

A.2900 Automated urinalysis system

import

Dates and Status

Apr 03, 2008

Apr 03, 2023

Sep 30, 2021

Cancellation Information

Logged out

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