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“GE” Giraffe Blue Spot PT Lite - Taiwan Registration 5ddcb6be395f588f456f49628876325e

Access comprehensive regulatory information for “GE” Giraffe Blue Spot PT Lite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ddcb6be395f588f456f49628876325e and manufactured by Lumitex Medical Devices, Inc.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, 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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5ddcb6be395f588f456f49628876325e
Registration Details
Taiwan FDA Registration: 5ddcb6be395f588f456f49628876325e
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Device Details

“GE” Giraffe Blue Spot PT Lite
TW: “奇異”新生兒光照射治療裝置
Risk Class 2
MD

Registration Details

5ddcb6be395f588f456f49628876325e

Ministry of Health Medical Device Import No. 029639

DHA05602963909

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J5700 Neonatal Light Irradiation Therapy Device

Imported from abroad

Dates and Status

Apr 18, 2017

Apr 18, 2027