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“Cynosure” Elite+ Laser - Taiwan Registration 8d5ea1afc4689f2c7a7263c022520e2d

Access comprehensive regulatory information for “Cynosure” Elite+ Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8d5ea1afc4689f2c7a7263c022520e2d and manufactured by CYNOSURE, LLC. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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8d5ea1afc4689f2c7a7263c022520e2d
Registration Details
Taiwan FDA Registration: 8d5ea1afc4689f2c7a7263c022520e2d
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Device Details

“Cynosure” Elite+ Laser
TW: “色若修”伊儷雷射
Risk Class 2
MD

Registration Details

8d5ea1afc4689f2c7a7263c022520e2d

Ministry of Health Medical Device Import No. 025599

DHA05602559903

Company Information

United States

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

Imported from abroad

Dates and Status

Nov 15, 2013

Nov 15, 2023