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Leishi Ophthalmic Erbium Chromium Laser - Taiwan Registration 788c86ec4a7f6aa73e1f1fecc8d75088

Access comprehensive regulatory information for Leishi Ophthalmic Erbium Chromium Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 788c86ec4a7f6aa73e1f1fecc8d75088 and manufactured by HOYA PHOTONICS, INC. D/B/A HOYA CONBIO;; ACE VISION GROUP. The authorized representative in Taiwan is VISION RENU CORPORATION.

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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788c86ec4a7f6aa73e1f1fecc8d75088
Registration Details
Taiwan FDA Registration: 788c86ec4a7f6aa73e1f1fecc8d75088
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Device Details

Leishi Ophthalmic Erbium Chromium Laser
TW: ็ฃŠ่ฆ–็œผ็ง‘้‰บ้›…้‰ป้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

788c86ec4a7f6aa73e1f1fecc8d75088

DHA00602217402

Company Information

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

Contract manufacturing;; input

Dates and Status

Feb 23, 2011

Feb 23, 2016

Jun 25, 2018

Cancellation Information

Logged out

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