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“Ming-mei” Cryotech Vitrification and Warming Kits - Taiwan Registration 8276154aec8d945769f53b871283d765

Access comprehensive regulatory information for “Ming-mei” Cryotech Vitrification and Warming Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8276154aec8d945769f53b871283d765 and manufactured by REPROLIFE Inc.. The authorized representative in Taiwan is MING-MEI TECHNOLOGY 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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8276154aec8d945769f53b871283d765
Registration Details
Taiwan FDA Registration: 8276154aec8d945769f53b871283d765
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Device Details

“Ming-mei” Cryotech Vitrification and Warming Kits
TW: “明美”卵與胚胎保存系統
Risk Class 2
MD

Registration Details

8276154aec8d945769f53b871283d765

Ministry of Health Medical Device Import No. 031835

DHA05603183501

Company Information

Japan

Product Details

For details, it is Chinese approved copy of the imitation order

l Devices for obstetrics and gynecology

L6180 Reproductive vehicles and supplements

Imported from abroad

Dates and Status

Oct 29, 2018

Oct 29, 2028