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"UNIPATH" Ovulation Test (Non-Sterile) - Taiwan Registration 62d3b8751fe8b22f1a84885f5fd5a1aa

Access comprehensive regulatory information for "UNIPATH" Ovulation 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 62d3b8751fe8b22f1a84885f5fd5a1aa and manufactured by UNIPATH LIMITED. The authorized representative in Taiwan is WEIYOU TECH INC..

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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62d3b8751fe8b22f1a84885f5fd5a1aa
Registration Details
Taiwan FDA Registration: 62d3b8751fe8b22f1a84885f5fd5a1aa
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Device Details

"UNIPATH" Ovulation Test (Non-Sterile)
TW: "ๅ„ชๅฆณไฝฉ" ๆŽ’ๅตๆธฌ่ฉฆ็ญ†(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

62d3b8751fe8b22f1a84885f5fd5a1aa

Ministry of Health Medical Device Import No. 014574

DHA09401457409

Company Information

United Kingdom

Product Details

A Clinical chemistry and clinical toxicology

A1485 Luteinizing Gonadotropin Test System

Imported from abroad

Dates and Status

Oct 15, 2014

Oct 15, 2019

Jun 22, 2022

Cancellation Information

Logged out

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