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"Pioneer" Euro 3 LED surgical light - Taiwan Registration c6dce22f5d881fc6b6484b1691dd108a

Access comprehensive regulatory information for "Pioneer" Euro 3 LED surgical light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6dce22f5d881fc6b6484b1691dd108a and manufactured by Skytron, LLC.; Dai-Ichi Shomei Co., Ltd.. The authorized representative in Taiwan is MEDIGIANT 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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c6dce22f5d881fc6b6484b1691dd108a
Registration Details
Taiwan FDA Registration: c6dce22f5d881fc6b6484b1691dd108a
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Device Details

"Pioneer" Euro 3 LED surgical light
TW: โ€œๅฒ้–‹ๅ‰ตโ€ๆญ็พ…3 LEDๅค–็ง‘ๆ‰‹่ก“็‡ˆ
Risk Class 2
Cancelled

Registration Details

c6dce22f5d881fc6b6484b1691dd108a

DHA05602596604

Company Information

United States;;Japan

Product Details

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

I General, Plastic Surgery and Dermatology

I.4580 Surgical lamp

Input;; Contract manufacturing

Dates and Status

Mar 05, 2014

Mar 05, 2019

Aug 05, 2022

Cancellation Information

Logged out

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