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"Liverage" Laser treatment instrument - Taiwan Registration 6115442ba2b1950e3bf204378b1a204a

Access comprehensive regulatory information for "Liverage" Laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6115442ba2b1950e3bf204378b1a204a and manufactured by LIVERAGE TECHNOLOGY INC.. The authorized representative in Taiwan is LIVERAGE BIOMEDICAL INC..

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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6115442ba2b1950e3bf204378b1a204a
Registration Details
Taiwan FDA Registration: 6115442ba2b1950e3bf204378b1a204a
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Device Details

"Liverage" Laser treatment instrument
TW: "ๅƒๆ‰" ้›ทๅฐ„ๆฒป็™‚ๅ„€
Risk Class 2
MD

Registration Details

6115442ba2b1950e3bf204378b1a204a

Ministry of Health Medical Device Manufacturing No. 005921

Company Information

Taiwan, Province of China

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Produced in Taiwan, China

Dates and Status

Nov 01, 2017

Nov 01, 2027