Taiwan FDA registration 998f271075d04cafd85b1e1aa6cbfa4b

ZEISS Corrective lenses (unsterilized) 

TW: 蔡司 矯正鏡片(未滅菌) 
Taiwan flagTaiwan·Risk Class 1·DAE MYUNG OPTICAL CO., LTD;; CARL ZEISS VISION INTERNATIONAL GMBH·Registered Dec 14, 2010 – Dec 14, 2015Cancelled
Registration details
Analysis ID
998f271075d04cafd85b1e1aa6cbfa4b
Customs Code
DHA04400962401
Company information
Manufacturer Country
Korea, Republic of;;Germany
Authorized Representative
Yakili Corporation of Agili
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5844 corrective lenses
Import Information
import
Dates and status
Registration Date
Dec 14, 2010
Expiry Date
Dec 14, 2015
Cancellation Date
Nov 16, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期;;自請註銷
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About this record

Access comprehensive regulatory information for ZEISS Corrective lenses (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 998f271075d04cafd85b1e1aa6cbfa4b and manufactured by DAE MYUNG OPTICAL CO., LTD;; CARL ZEISS VISION INTERNATIONAL GMBH. The authorized representative in Taiwan is Yakili Corporation of Agili.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS VISION INTERNATIONAL GMBH;; CARL ZEISS VISION TECHNICAL SERVICES GUANGZHOU LTD., 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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