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“Veol” VERSATOR Tissue Morcellation System - Taiwan Registration d3a5b2b772cc0947bbdd07f764815824

Access comprehensive regulatory information for “Veol” VERSATOR Tissue Morcellation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3a5b2b772cc0947bbdd07f764815824 and manufactured by Veol Medical Technologies Pvt. Ltd.. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., 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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d3a5b2b772cc0947bbdd07f764815824
Registration Details
Taiwan FDA Registration: d3a5b2b772cc0947bbdd07f764815824
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Device Details

“Veol” VERSATOR Tissue Morcellation System
TW: “威爾”組織切除系統
Risk Class 2
MD

Registration Details

d3a5b2b772cc0947bbdd07f764815824

Ministry of Health Medical Device Import No. 033795

DHA05603379502

Company Information

Product Details

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

l Devices for obstetrics and gynecology

L1720 Laparoscopy for obstetrics and gynecology and its accessories

Imported from abroad

Dates and Status

Jul 16, 2020

Jul 16, 2025