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Vitrolife andrology system - Taiwan Registration 07b080f5d9a9f7ae0966016a6e61e50c

Access comprehensive regulatory information for Vitrolife andrology system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07b080f5d9a9f7ae0966016a6e61e50c and manufactured by Vitrolife Sweden AB. The authorized representative in Taiwan is TSENG HSIANG LIFE SCIENCE 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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07b080f5d9a9f7ae0966016a6e61e50c
Registration Details
Taiwan FDA Registration: 07b080f5d9a9f7ae0966016a6e61e50c
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Device Details

Vitrolife andrology system
TW: ๅฏ†้™€ไพ†็ฆ็”ทๆ€ง็”Ÿๆฎ–ๅŸน้คŠ็ณป็ตฑ
Risk Class 2
MD

Registration Details

07b080f5d9a9f7ae0966016a6e61e50c

Ministry of Health Medical Device Import No. 028604

DHA05602860401

Company Information

Sweden

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

Jun 13, 2016

Jun 13, 2026