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Vitrolife Follicle Aspiration Set - Taiwan Registration f5d2fd48a8388ec23035ac64bdd3ad0f

Access comprehensive regulatory information for Vitrolife Follicle Aspiration Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f5d2fd48a8388ec23035ac64bdd3ad0f 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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f5d2fd48a8388ec23035ac64bdd3ad0f
Registration Details
Taiwan FDA Registration: f5d2fd48a8388ec23035ac64bdd3ad0f
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Device Details

Vitrolife Follicle Aspiration Set
TW: ๅฏ†้™€ไพ†็ฆๅ–ๅต้‡
Risk Class 2
MD

Registration Details

f5d2fd48a8388ec23035ac64bdd3ad0f

Ministry of Health Medical Device Import No. 027295

DHA05602729506

Company Information

Sweden

Product Details

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

l Devices for obstetrics and gynecology

L6100 Guide needle for assisted reproduction

Imported from abroad

Dates and Status

May 18, 2015

May 18, 2025