Taiwan FDA registration 5ea505ef0da99ba4bd3b78055e9bc1aa

Tenger corrective lenses (unsterilized)

TW: "天格" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DANYANG LENS OPTICS TECHNOLOGY CO., LTD.·Registered Aug 22, 2017 – Aug 22, 2022Cancelled
Registration details
Analysis ID
5ea505ef0da99ba4bd3b78055e9bc1aa
Customs Code
DHA09600318707
Company information
Manufacturer Country
China
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
Chinese goods;; input
Dates and status
Registration Date
Aug 22, 2017
Expiry Date
Aug 22, 2022
Cancellation Date
Apr 12, 2024
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 Tenger 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 5ea505ef0da99ba4bd3b78055e9bc1aa and manufactured by DANYANG LENS OPTICS TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is TGT HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including F&F OPTICAL (SHANGHAI) CO., LTD, SHANGHAI PINDE OPTICAL GLASSES CO., LTD, and 5 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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