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“Ellipse A/S” Intense Pulsed Light System - Taiwan Registration 1c87369be22e6c91bf0b044afce0f4e3

Access comprehensive regulatory information for “Ellipse A/S” Intense Pulsed Light System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c87369be22e6c91bf0b044afce0f4e3 and manufactured by ELLIPSE A/S. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES 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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1c87369be22e6c91bf0b044afce0f4e3
Registration Details
Taiwan FDA Registration: 1c87369be22e6c91bf0b044afce0f4e3
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Device Details

“Ellipse A/S” Intense Pulsed Light System
TW: “丹麥”愛爾脈衝光系統
Risk Class 2
MD

Registration Details

1c87369be22e6c91bf0b044afce0f4e3

Ministry of Health Medical Device Import No. 025497

DHA05602549708

Company Information

Denmark

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

Oct 10, 2013

Oct 10, 2023