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“Skytron” AURORA 4 LED Surgical Lights - Taiwan Registration d2bb718f63d136f2ed9205828048f0e8

Access comprehensive regulatory information for “Skytron” AURORA 4 LED Surgical Lights in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2bb718f63d136f2ed9205828048f0e8 and manufactured by Dai-Ichi Shomei Co., Ltd.. The authorized representative in Taiwan is SYM-MED 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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d2bb718f63d136f2ed9205828048f0e8
Registration Details
Taiwan FDA Registration: d2bb718f63d136f2ed9205828048f0e8
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Device Details

“Skytron” AURORA 4 LED Surgical Lights
TW: “司凱壯”色溫可調發光二極體手術燈
Risk Class 2
MD

Registration Details

d2bb718f63d136f2ed9205828048f0e8

Ministry of Health Medical Device Import No. 030689

DHA05603068901

Company Information

Japan

Product Details

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

I General and plastic surgical devices

I4580 Surgical light

Imported from abroad

Dates and Status

Jan 16, 2018

Jan 16, 2028