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"WWIN WAY" KERATOSCOPE (Non-Sterile) - Taiwan Registration a2d58bd40124e2d53857ad66e873229d

Access comprehensive regulatory information for "WWIN WAY" KERATOSCOPE (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2d58bd40124e2d53857ad66e873229d and manufactured by NEW VISION PROTECT LASERSHUTZ GMBH. The authorized representative in Taiwan is WWIN WAY TECHNOLOGY CO., LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NEW VISION PROTECT LASERSHUTZ GMBH, and 1 recent registrations in the same category. 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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a2d58bd40124e2d53857ad66e873229d
Registration Details
Taiwan FDA Registration: a2d58bd40124e2d53857ad66e873229d
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Device Details

"WWIN WAY" KERATOSCOPE (Non-Sterile)
TW: ่ฌ่ƒฝ่ง’่†œ้ก (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

a2d58bd40124e2d53857ad66e873229d

Ministry of Health Medical Device Import No. 021378

DHA09402137800

Company Information

Product Details

M Ophthalmic devices

M1350 Keatoscope

Imported from abroad

Dates and Status

Mar 18, 2020

Mar 18, 2025

Cancellation Information

Logged out

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