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“DEKA” HIRO Nd YAG Laser Therapy Apparatus - Taiwan Registration ea17ac9b0992da57db69a844d0b29927

Access comprehensive regulatory information for “DEKA” HIRO Nd YAG Laser 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 ea17ac9b0992da57db69a844d0b29927 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is GAIA GENOMICS CORP..

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ea17ac9b0992da57db69a844d0b29927
Registration Details
Taiwan FDA Registration: ea17ac9b0992da57db69a844d0b29927
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Device Details

“DEKA” HIRO Nd YAG Laser Therapy Apparatus
TW: “德卡”喜樂雷射治療儀
Risk Class 2
MD

Registration Details

ea17ac9b0992da57db69a844d0b29927

Ministry of Health Medical Device Import No. 028537

DHA05602853709

Company Information

Italy

Product Details

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

o Equipment for physical medicine

O5500 infrared light

Imported from abroad

Dates and Status

May 17, 2016

May 17, 2026