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Rhence Langliv - Taiwan Registration 3171599b10beeeb6e1c2e24d0a620086

Access comprehensive regulatory information for Rhence Langliv in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3171599b10beeeb6e1c2e24d0a620086 and manufactured by Q-MED AB. The authorized representative in Taiwan is GALDERMA HONG KONG LIMITED, TAIWAN BRANCH.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Q-MED 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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3171599b10beeeb6e1c2e24d0a620086
Registration Details
Taiwan FDA Registration: 3171599b10beeeb6e1c2e24d0a620086
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Device Details

Rhence Langliv
TW: ็‘ž็ตฒๆœ—้บ—่Š™
Risk Class 3

Registration Details

3171599b10beeeb6e1c2e24d0a620086

DHA00602189102

Company Information

Sweden

Product Details

Details are Chinese Approved Version of Generic Orders; Effect of Changes on June 4, 101: Details as Chinese Approved Copies of Generic Orders, blank below.

I General, Plastic Surgery and Dermatology

import

Dates and Status

Mar 24, 2020

Dec 29, 2025

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