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“EFB” Intense Pulsed Light - Taiwan Registration 658c3ebe1460577e13bdc7f4ebaed528

Access comprehensive regulatory information for “EFB” Intense 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 658c3ebe1460577e13bdc7f4ebaed528 and manufactured by EUROFEEDBACK SAS. The authorized representative in Taiwan is CROWNMED ENTERPRISE 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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658c3ebe1460577e13bdc7f4ebaed528
Registration Details
Taiwan FDA Registration: 658c3ebe1460577e13bdc7f4ebaed528
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Device Details

“EFB” Intense Pulsed Light
TW: “伊膚寶”脈衝光治療儀
Risk Class 2
MD
Cancelled

Registration Details

658c3ebe1460577e13bdc7f4ebaed528

Ministry of Health Medical Device Import No. 026785

DHA05602678505

Company Information

France

Product Details

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Nov 17, 2014

Nov 17, 2019

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期