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"Intermedi" Andu laser diode - Taiwan Registration 0f2a6e429bf99aa4ff96f3558f5cd08f

Access comprehensive regulatory information for "Intermedi" Andu laser diode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f2a6e429bf99aa4ff96f3558f5cd08f and manufactured by INTERMEDIC ARFRAN, S.A.. The authorized representative in Taiwan is Yifeng International Enterprises Limited.

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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0f2a6e429bf99aa4ff96f3558f5cd08f
Registration Details
Taiwan FDA Registration: 0f2a6e429bf99aa4ff96f3558f5cd08f
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Device Details

"Intermedi" Andu laser diode
TW: โ€œๅ› ็‰น็พŽๅœฐโ€ๅฎ‰ๅบฆ้›ทๅฐ„ไบŒๆฅตๅ„€
Risk Class 2
Cancelled

Registration Details

0f2a6e429bf99aa4ff96f3558f5cd08f

DHA00602300408

Company Information

Spain

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

Nov 09, 2011

Nov 09, 2016

Mar 14, 2016

Cancellation Information

Logged out

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