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“DEKA” EXCILITE ULTRAVIOLET-THERAPY APPARATUS - Taiwan Registration bdd0cbb17fabde81d08089d7b3060a79

Access comprehensive regulatory information for “DEKA” EXCILITE ULTRAVIOLET-THERAPY APPARATUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bdd0cbb17fabde81d08089d7b3060a79 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA 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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bdd0cbb17fabde81d08089d7b3060a79
Registration Details
Taiwan FDA Registration: bdd0cbb17fabde81d08089d7b3060a79
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Device Details

“DEKA” EXCILITE ULTRAVIOLET-THERAPY APPARATUS
TW: “德卡”紫外線治療器
Risk Class 2
MD

Registration Details

bdd0cbb17fabde81d08089d7b3060a79

Ministry of Health Medical Device Import No. 031181

DHA05603118106

Company Information

Italy

Product Details

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

I General and plastic surgical devices

I4630 UV lamp for dermatology

Imported from abroad

Dates and Status

Jun 12, 2018

Jun 12, 2028