Taiwan FDA registration b4ef31ca9072a7f6c0c4b5b6265d9952

"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 Apr 13, 2010 – Apr 13, 2015Cancelled
Registration details
Analysis ID
b4ef31ca9072a7f6c0c4b5b6265d9952
Customs Code
DHA04400871101
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
Apr 13, 2010
Expiry Date
Apr 13, 2015
Cancellation Date
May 21, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 b4ef31ca9072a7f6c0c4b5b6265d9952 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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