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"Arthur" Guinenine infrared laser treatment device - Taiwan Registration 2b62dca9aa2aa049ab4dbb9474160d0a

Access comprehensive regulatory information for "Arthur" Guinenine infrared laser treatment device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b62dca9aa2aa049ab4dbb9474160d0a and manufactured by ASA 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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2b62dca9aa2aa049ab4dbb9474160d0a
Registration Details
Taiwan FDA Registration: 2b62dca9aa2aa049ab4dbb9474160d0a
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Device Details

"Arthur" Guinenine infrared laser treatment device
TW: โ€œไบž็‘Ÿโ€ๅฅๅŠ›้ฉ็ด…ๅค–็ทš้›ทๅฐ„ๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

2b62dca9aa2aa049ab4dbb9474160d0a

DHA05603339407

Company Information

Italy

Product Details

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

o Physical Medical Sciences;; I General, Plastic Surgery and Dermatology

O.5500 Infrared lamp;; I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

Mar 14, 2020

Mar 14, 2030