Taiwan FDA registration a2d58bd40124e2d53857ad66e873229d

"WWIN WAY" KERATOSCOPE (Non-Sterile)

TW: 萬能角膜鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·NEW VISION PROTECT LASERSHUTZ GMBH·Registered Mar 18, 2020 – Mar 18, 2025Cancelled
Registration details
Analysis ID
a2d58bd40124e2d53857ad66e873229d
License Form
Ministry of Health Medical Device Import No. 021378
Customs Code
DHA09402137800
Company information
Manufacturer Country
Germany
Authorized Representative
WWIN WAY TECHNOLOGY CO., LTD
Product details
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 18, 2020
Expiry Date
Mar 18, 2025
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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