Taiwan FDA registration 666cac97c98cadcaca0339431cee1cc8

Manual Ophthalmic Surgery Instrument (Sterile)

TW: "特諾美" 手動式眼科手術器械 (滅菌)
Taiwan flagTaiwan·Risk Class 1·TEKNOMEK MEDICAL MATERIALS INDUSTRY AND TRADE LTD. STI·Registered Jan 02, 2019 – Jan 02, 2029Active
Registration details
Analysis ID
666cac97c98cadcaca0339431cee1cc8
Customs Code
DHA09401998503
Company information
Manufacturer Country
Türkiye
Authorized Representative
CRYSTALVISION CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4350 手動式眼科手術器械
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Jan 02, 2019
Expiry Date
Jan 02, 2029
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About this record

Access comprehensive regulatory information for Manual Ophthalmic Surgery Instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 666cac97c98cadcaca0339431cee1cc8 and manufactured by TEKNOMEK MEDICAL MATERIALS INDUSTRY AND TRADE LTD. STI. The authorized representative in Taiwan is CRYSTALVISION CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including CARL ZEISS MEDITEC AG;; COASTLINE DE MEXICO, S.A. DE C.V., BAUSCH & LOMB INC.;; SURGICAL SPECIALTIES MEXICO, S. DE R.L. DE C.V., 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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