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“ARC” Diode Laser Wolf - Taiwan Registration eefe087e7b6105257b51fb202915d415

Access comprehensive regulatory information for “ARC” Diode Laser Wolf in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eefe087e7b6105257b51fb202915d415 and manufactured by A.R.C. Laser GmbH. The authorized representative in Taiwan is PAXUAN 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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eefe087e7b6105257b51fb202915d415
Registration Details
Taiwan FDA Registration: eefe087e7b6105257b51fb202915d415
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Device Details

“ARC” Diode Laser Wolf
TW: “亞爾斯”沃夫二極體雷射系統
Risk Class 2
MD

Registration Details

eefe087e7b6105257b51fb202915d415

Ministry of Health Medical Device Import No. 036431

DHA05603643102

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Mar 09, 2023

Mar 09, 2028