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"Xingchang" light nasal organ - Taiwan Registration 3cef155a263de8f237021aae8df4c12e

Access comprehensive regulatory information for "Xingchang" light nasal organ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3cef155a263de8f237021aae8df4c12e and manufactured by Changzhou Biolight Medical Devices Co., Ltd.;; Biolight Medical Devices Ltd.. The authorized representative in Taiwan is HI-CLEARANCE 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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3cef155a263de8f237021aae8df4c12e
Registration Details
Taiwan FDA Registration: 3cef155a263de8f237021aae8df4c12e
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Device Details

"Xingchang" light nasal organ
TW: โ€œๆๆ˜Œโ€ๅ…‰้ผปๅ™จ
Risk Class 2

Registration Details

3cef155a263de8f237021aae8df4c12e

DHA09200141402

Company Information

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Input;; Chinese goods;; Contract manufacturing

Dates and Status

Oct 13, 2022

Oct 13, 2027