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"Apo" IVF micromanipulation tube - Taiwan Registration 7835e1f346ebdcecbe5ce8db2a862878

Access comprehensive regulatory information for "Apo" IVF micromanipulation tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7835e1f346ebdcecbe5ce8db2a862878 and manufactured by Vitrolife Sweden AB. The authorized representative in Taiwan is unitedparadise technology Limited.

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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7835e1f346ebdcecbe5ce8db2a862878
Registration Details
Taiwan FDA Registration: 7835e1f346ebdcecbe5ce8db2a862878
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Device Details

"Apo" IVF micromanipulation tube
TW: โ€œไบžๆจธโ€ ้ซ”ๅค–ๅ—็ฒพ้กฏๅพฎๆ“ไฝœ็ฎก
Risk Class 2

Registration Details

7835e1f346ebdcecbe5ce8db2a862878

DHA05603727302

Company Information

Sweden

Product Details

Details are as detailed as approved Chinese instructions

l Obstetrics and Gynecology

L.6130 ่ผ”ๅŠฉ็”Ÿๆฎ–ไน‹ๅพฎๅฐๅ™จๅ…ท

import

Dates and Status

Aug 07, 2024

Aug 07, 2029