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"Guandalla" diode laser system and accessories - Taiwan Registration aa1f7c46a70ea1bd2b10f3c71cc50b6a

Access comprehensive regulatory information for "Guandalla" diode laser system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa1f7c46a70ea1bd2b10f3c71cc50b6a and manufactured by Quanta System S.p.A. The authorized representative in Taiwan is KUAN FWA MED 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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aa1f7c46a70ea1bd2b10f3c71cc50b6a
Registration Details
Taiwan FDA Registration: aa1f7c46a70ea1bd2b10f3c71cc50b6a
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Device Details

"Guandalla" diode laser system and accessories
TW: โ€œ่ฒซ้”ๆจ‚โ€ไบŒๆฅต้ซ”้›ทๅฐ„็ณป็ตฑๅŠ้…ไปถ
Risk Class 2

Registration Details

aa1f7c46a70ea1bd2b10f3c71cc50b6a

DHA05603031203

Company Information

Italy

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

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input

Dates and Status

Sep 28, 2017

Sep 28, 2027