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"FRASTEMA" Ophthalmic Trial Lens Set (Non-Sterile) - Taiwan Registration b9099e4f90709b9e7d2b3746c5c09b1a

Access comprehensive regulatory information for "FRASTEMA" Ophthalmic Trial Lens Set (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 b9099e4f90709b9e7d2b3746c5c09b1a and manufactured by FRASTEMA S.R.L.. The authorized representative in Taiwan is CLINICO INC..

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.

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b9099e4f90709b9e7d2b3746c5c09b1a
Registration Details
Taiwan FDA Registration: b9099e4f90709b9e7d2b3746c5c09b1a
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Device Details

"FRASTEMA" Ophthalmic Trial Lens Set (Non-Sterile)
TW: "่ฒปๆ–ฏ็‰น"็œผ็ง‘่ฉฆ้ฉ—้ก็‰‡็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b9099e4f90709b9e7d2b3746c5c09b1a

Ministry of Health Medical Device Import No. 022735

DHA09402273503

Company Information

Italy

Product Details

Limited to the classification and grading management method of medical equipment, the first level recognition range of the ophthalmic test lens group (M.1405).

M Ophthalmology

M1405 Ophthalmic Test Lens Group

Imported from abroad

Dates and Status

Jan 22, 2022

Jan 22, 2027