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"LensHooke" Sperm Separation Device - Taiwan Registration 74e511a501ba88ce383691f83df3306d

Access comprehensive regulatory information for "LensHooke" Sperm Separation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74e511a501ba88ce383691f83df3306d 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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74e511a501ba88ce383691f83df3306d
Registration Details
Taiwan FDA Registration: 74e511a501ba88ce383691f83df3306d
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Device Details

"LensHooke" Sperm Separation Device
TW: "่Š็‰นๅ…’" ็ฒพๅญๅ„ช้ธๅ™จ
Risk Class 2
MD

Registration Details

74e511a501ba88ce383691f83df3306d

Ministry of Health Medical Device Manufacturing No. 007780

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

l Obstetrics and Gynecology

L6160 Laboratory equipment for assisted reproduction

Produced in Taiwan, China

Dates and Status

Dec 11, 2022

Dec 11, 2027