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Vitrolife Micromanipulation Pipettes - Taiwan Registration 925fb5941647f4ba4ac0bd2ee85c88ca

Access comprehensive regulatory information for Vitrolife Micromanipulation Pipettes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 925fb5941647f4ba4ac0bd2ee85c88ca 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, 1 companies making similar products including Vitrolife Inc., and 1 recent registrations in the same category. 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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925fb5941647f4ba4ac0bd2ee85c88ca
Registration Details
Taiwan FDA Registration: 925fb5941647f4ba4ac0bd2ee85c88ca
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Device Details

Vitrolife Micromanipulation Pipettes
TW: ๅฏ†้™€ไพ†็ฆ้ซ”ๅค–ๅ—็ฒพ้กฏๅพฎๆ“ไฝœ็ฎก
Risk Class 2
MD

Registration Details

925fb5941647f4ba4ac0bd2ee85c88ca

Ministry of Health Medical Device Import No. 027304

DHA05602730407

Company Information

Sweden

Product Details

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

l Devices for obstetrics and gynecology

L6130 Tiny apparatus for assisted reproduction

Imported from abroad

Dates and Status

May 26, 2015

May 26, 2025

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