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"Shapaulette" Fuller pulsed light - Taiwan Registration 76a42c615ed10c797926c1fbfa3ecc53

Access comprehensive regulatory information for "Shapaulette" Fuller pulsed light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76a42c615ed10c797926c1fbfa3ecc53 and manufactured by Sharplight Technologies Ltd. The authorized representative in Taiwan is COLLAMATRIX 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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76a42c615ed10c797926c1fbfa3ecc53
Registration Details
Taiwan FDA Registration: 76a42c615ed10c797926c1fbfa3ecc53
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Device Details

"Shapaulette" Fuller pulsed light
TW: โ€œๅคๆ™ฎ่Š็‰นโ€้ฆฅ็พŽ่„ˆ่กๅ…‰
Risk Class 2
Cancelled

Registration Details

76a42c615ed10c797926c1fbfa3ecc53

DHA05602901204

Company Information

Israel

Product Details

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

I General, Plastic Surgery and Dermatology

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

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Nov 03, 2016

Nov 03, 2021

Aug 15, 2023

Cancellation Information

Logged out

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