Taiwan FDA registration 78eec67e16b8cbd7362ac33b1ea5bb4e

Gao Bo Feiteng corrective lenses (unsterilized)

TW: 高峰博飛騰矯正鏡片(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Shanghai Lantern Optics Co.,Ltd·Registered Nov 17, 2022 – Nov 17, 2027Active
Registration details
Analysis ID
78eec67e16b8cbd7362ac33b1ea5bb4e
Customs Code
DHA09600469505
Company information
Manufacturer Country
China
Authorized Representative
Perfect Vision Co., Ltd.
Product details
Intended Use
Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.5844 corrective lenses
Import Information
Chinese goods;; input
Dates and status
Registration Date
Nov 17, 2022
Expiry Date
Nov 17, 2027
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About this record

Access comprehensive regulatory information for Gao Bo Feiteng 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 78eec67e16b8cbd7362ac33b1ea5bb4e and manufactured by Shanghai Lantern Optics Co.,Ltd. The authorized representative in Taiwan is Perfect Vision Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JunePei Optical Co., Ltd.;; Bofeiteng Optical Co., 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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