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Vitrolife Micromanipulation Pipettes - Taiwan Registration 0991124e20be6c98869187195a4efe7c

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 0991124e20be6c98869187195a4efe7c and manufactured by Vitrolife Inc.. 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 Sweden AB, 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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0991124e20be6c98869187195a4efe7c
Registration Details
Taiwan FDA Registration: 0991124e20be6c98869187195a4efe7c
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Device Details

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

Registration Details

0991124e20be6c98869187195a4efe7c

Ministry of Health Medical Device Import No. 027027

DHA05602702707

Company Information

United States

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

Feb 26, 2015

Feb 26, 2025

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