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“LEONI” Laser Fiber - Taiwan Registration f550e85d546b109c7dfb3e992eb0004d

Access comprehensive regulatory information for “LEONI” Laser Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f550e85d546b109c7dfb3e992eb0004d and manufactured by LEONI Fiber Optics, Inc.. The authorized representative in Taiwan is SMARTECH MEDICAL 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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f550e85d546b109c7dfb3e992eb0004d
Registration Details
Taiwan FDA Registration: f550e85d546b109c7dfb3e992eb0004d
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Device Details

“LEONI” Laser Fiber
TW: “雷奧尼”雷射光纖
Risk Class 2
MD

Registration Details

f550e85d546b109c7dfb3e992eb0004d

Ministry of Health Medical Device Import No. 036128

DHA05603612801

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Dec 13, 2022

Dec 13, 2027