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"Addomon" neonatal phototherapy device - Taiwan Registration 202f3e92bc446b1b7e5c0c261e57dc75

Access comprehensive regulatory information for "Addomon" neonatal phototherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 202f3e92bc446b1b7e5c0c261e57dc75 and manufactured by Atom Medical Corporation Urawa Factory. The authorized representative in Taiwan is PROMED INSTRUMENT 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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202f3e92bc446b1b7e5c0c261e57dc75
Registration Details
Taiwan FDA Registration: 202f3e92bc446b1b7e5c0c261e57dc75
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Device Details

"Addomon" neonatal phototherapy device
TW: โ€œไบžๅคš่’™โ€ๆ–ฐ็”Ÿๅ…’ๅ…‰็…งๆฒป็™‚่ฃ็ฝฎ
Risk Class 2

Registration Details

202f3e92bc446b1b7e5c0c261e57dc75

DHA00602484902

Company Information

Product Details

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

J General hospital and personal use equipment

J.5700 Neonatal light therapy device

import

Dates and Status

Apr 12, 2013

Apr 12, 2028