Taiwan FDA registration a00dafeb7d49b3461c5859de464952fa

"Kowa Company" Vision Tester and Accessories (Non-Sterile)

TW: "興和" 視力檢查儀及附件 (未滅菌)

Taiwan·Risk Class 1·MD·KOWA COMPANY, LTD.·Registered Feb 05, 2021 – Feb 05, 2026Expired

Registration details

Analysis ID: a00dafeb7d49b3461c5859de464952fa
License Form: Ministry of Health Medical Device Import No. 022301
Customs Code: DHA09402230109

Company information

Manufacturer: KOWA COMPANY, LTD.
Manufacturer Country: Japan
Authorized Representative: EVERVISION INSTRUMENT CO.

Product details

Intended Use: Limited to the first level recognition range of ophthalmic projectors (M.1680) for the management of medical equipment.
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M1680 Ophthalmic Projector
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 05, 2021
Expiry Date: Feb 05, 2026

About this record

Access comprehensive regulatory information for "Kowa Company" Vision Tester and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a00dafeb7d49b3461c5859de464952fa and manufactured by KOWA COMPANY, LTD.. The authorized representative in Taiwan is EVERVISION INSTRUMENT CO..

This page provides complete technical specifications, regulatory compliance details. 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.