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LensHooke Sperm DNA Fragmentation Test Kit (Non-Sterile) - Taiwan Registration 5cc861bc0ebd301522e3efef6fa8c230

Access comprehensive regulatory information for LensHooke Sperm DNA Fragmentation Test Kit (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 5cc861bc0ebd301522e3efef6fa8c230 and manufactured by BONRAYBIO CO., LTD.. The authorized representative in Taiwan is BONRAYBIO 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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5cc861bc0ebd301522e3efef6fa8c230
Registration Details
Taiwan FDA Registration: 5cc861bc0ebd301522e3efef6fa8c230
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Device Details

LensHooke Sperm DNA Fragmentation Test Kit (Non-Sterile)
TW: ่Š็‰นๅ…’็ฒพๅญๆŸ“่‰ฒ่ฉฆๅŠ‘ๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

5cc861bc0ebd301522e3efef6fa8c230

Ministry of Health Medical Device Manufacturing No. 008723

Company Information

Taiwan, Province of China

Product Details

B Hematology and pathology devices

B1850 Dyes and chemical solution dyes

Produced in Taiwan, China

Dates and Status

Dec 11, 2020

Dec 11, 2025

Cancellation Information

Logged out

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