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"Dirui" urine analyzer (unsterilized) - Taiwan Registration f63f6ddd16986bed7bffb18311c400fa

Access comprehensive regulatory information for "Dirui" 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 f63f6ddd16986bed7bffb18311c400fa and manufactured by DIRUI INDUSTRIAL CO., LTD.. The authorized representative in Taiwan is TENG SIH ENTERPRISE COMPANY LIMITED.

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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f63f6ddd16986bed7bffb18311c400fa
Registration Details
Taiwan FDA Registration: f63f6ddd16986bed7bffb18311c400fa
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Device Details

"Dirui" urine analyzer (unsterilized)
TW: "่ฟช็‘ž" ๅฐฟๆถฒๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f63f6ddd16986bed7bffb18311c400fa

DHA09600245402

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

A.2900 Automated urinalysis system

QMS/QSD;; Input;; Chinese goods

Dates and Status

Jul 20, 2015

Jul 20, 2020

Jun 22, 2022

Cancellation Information

Logged out

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