Taiwan FDA registration 679ce9a06e1f3926752835fd4566cf17

"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 Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
679ce9a06e1f3926752835fd4566cf17
License Form
Ministry of Health Medical Device Import Registration No. 021378
Customs Code
DHA08402137804
Company information
Manufacturer Country
Germany
Authorized Representative
WWIN WAY TECHNOLOGY CO., LTD
Product details
Intended Use
Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M1350 Keatoscope
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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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 679ce9a06e1f3926752835fd4566cf17 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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