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“DEKA” SH1 Nd YAG Laser Therapy Apparatus - Taiwan Registration 6ffaac7c411e1b4a5626d93a506bab1f

Access comprehensive regulatory information for “DEKA” SH1 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 6ffaac7c411e1b4a5626d93a506bab1f and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is GAIA GENOMICS CORP..

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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6ffaac7c411e1b4a5626d93a506bab1f
Registration Details
Taiwan FDA Registration: 6ffaac7c411e1b4a5626d93a506bab1f
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Device Details

“DEKA” SH1 Nd YAG Laser Therapy Apparatus
TW: “德卡”喜望雷射治療儀
Risk Class 2
MD

Registration Details

6ffaac7c411e1b4a5626d93a506bab1f

Ministry of Health Medical Device Import No. 030168

DHA05603016809

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

Aug 31, 2017

Aug 31, 2027