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"Leoni" medical laser fiber - Taiwan Registration a97a6519b305293142a6d3d456e8f3a1

Access comprehensive regulatory information for "Leoni" medical laser fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a97a6519b305293142a6d3d456e8f3a1 and manufactured by LEONI Fiber Optics GmbH. The authorized representative in Taiwan is INNOMED INTERNATIONAL INC..

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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a97a6519b305293142a6d3d456e8f3a1
Registration Details
Taiwan FDA Registration: a97a6519b305293142a6d3d456e8f3a1
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Device Details

"Leoni" medical laser fiber
TW: โ€œ่•พๆญๅฐผโ€้†ซ็”จ้›ทๅฐ„ๅ…‰็บ–
Risk Class 2

Registration Details

a97a6519b305293142a6d3d456e8f3a1

DHA00602473003

Company Information

Germany

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

Feb 06, 2013

Feb 06, 2023