Taiwan FDA registration 723db63859027a1d49256deda8b06ecd

"Weiweilai" ophthalmic refractive machine (unsterilized)

TW: "威微賴" 眼科驗光機 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·WAVELIGHT GMBH·Registered Oct 17, 2011 – Oct 17, 2016Cancelled
Registration details
Analysis ID
723db63859027a1d49256deda8b06ecd
Customs Code
DHA04401094709
Company information
Manufacturer
WAVELIGHT GMBH
Manufacturer Country
Germany
Product details
Intended Use
Limited to the first level recognition range of ophthalmic optometry machine (M.1760) of the management measures for medical equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.1760 Automatic Ophthalmic Optical Machine
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Oct 17, 2011
Expiry Date
Oct 17, 2016
Cancellation Date
Sep 26, 2016
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Weiweilai" ophthalmic refractive machine (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 723db63859027a1d49256deda8b06ecd and manufactured by WAVELIGHT GMBH. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including WAVELIGHT 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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