Taiwan FDA registration 649e2cd3b6f1e55cbcf5bf4935847f1b

"FE-GROUP" Ophthalmic trial lens set (non-sterile)

TW: "菲葛" 眼科試驗鏡片組 (未滅菌)

Taiwan·Risk Class 1·MD·FE-Group srl·Registered Dec 30, 2022 – Dec 30, 2027Active

Registration details

Analysis ID: 649e2cd3b6f1e55cbcf5bf4935847f1b
License Form: Ministry of Health Medical Device Import No. 022996
Customs Code: DHA09402299605

Company information

Manufacturer: FE-Group srl
Manufacturer Country: Italy
Authorized Representative: JUN FENG OPTICAL CO., LTD.

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: Dec 30, 2022
Expiry Date: Dec 30, 2027

About this record

Access comprehensive regulatory information for "FE-GROUP" 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 649e2cd3b6f1e55cbcf5bf4935847f1b and manufactured by FE-Group srl. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..

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