Taiwan FDA registration b9099e4f90709b9e7d2b3746c5c09b1a

"FRASTEMA" Ophthalmic Trial Lens Set (Non-Sterile)

TW: "費斯特"眼科試驗鏡片組(未滅菌)

Taiwan·Risk Class 1·MD·FRASTEMA S.R.L.·Registered Jan 22, 2022 – Jan 22, 2027Active

Registration details

Analysis ID: b9099e4f90709b9e7d2b3746c5c09b1a
License Form: Ministry of Health Medical Device Import No. 022735
Customs Code: DHA09402273503

Company information

Manufacturer: FRASTEMA S.R.L.
Manufacturer Country: Italy
Authorized Representative: CLINICO INC.

Product details

Intended Use: Limited to the classification and grading management method of medical equipment, the first level recognition range of the ophthalmic test lens group (M.1405).
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M1405 Ophthalmic Test Lens Group
Import Information: Imported from abroad

Dates and status

Registration Date: Jan 22, 2022
Expiry Date: Jan 22, 2027

About this record

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..

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