Taiwan FDA registration b1cda4f0d7b2f7c24f159e2311d87de8

Test lens clip lens group according to the optic path (unsterilized)

TW: 依視路試驗鏡片夾鏡片組(未滅菌)

Taiwan·Risk Class 1·ESSILOR INTERNATIONAL·Registered Apr 19, 2022 – Apr 19, 2027Active

Registration details

Analysis ID: b1cda4f0d7b2f7c24f159e2311d87de8
Customs Code: DHA09402278403

Company information

Manufacturer: ESSILOR INTERNATIONAL
Manufacturer Country: France
Authorized Representative: ESSILOR-POLYLITE TAIWAN CO., LTD.

Product details

Intended Use: Limited to the classification and grading management of medical equipment, the first level identification range of ophthalmic test lens group (M.1405) and ophthalmic test lens clip (M.1410).
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.1410 眼科試驗鏡片夾;; M.1405 眼科試驗鏡片組
Import Information: import

Dates and status

Registration Date: Apr 19, 2022
Expiry Date: Apr 19, 2027

About this record

Access comprehensive regulatory information for Test lens clip lens group according to the optic path (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1cda4f0d7b2f7c24f159e2311d87de8 and manufactured by ESSILOR INTERNATIONAL. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

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.