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“Pollogen” DIVINE Pro System - Taiwan Registration daecc10479ea4b266ac48b2a898b97d3

Access comprehensive regulatory information for “Pollogen” DIVINE Pro System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number daecc10479ea4b266ac48b2a898b97d3 and manufactured by Pollogen Ltd.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.

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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daecc10479ea4b266ac48b2a898b97d3
Registration Details
Taiwan FDA Registration: daecc10479ea4b266ac48b2a898b97d3
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Device Details

“Pollogen” DIVINE Pro System
TW: “博樂金”德邁電波除皺系統
Risk Class 2
MD

Registration Details

daecc10479ea4b266ac48b2a898b97d3

Ministry of Health Medical Device Import No. 035065

DHA05603506501

Company Information

Israel

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4400 Electric knife for cutting and hemostasis and its accessories

Imported from abroad

Dates and Status

Nov 22, 2021

Nov 22, 2026