Taiwan FDA registration a343877fa1c09ed330b0298bb792d2f5

"Luneau" Ophthalmic trial lens set (Non-Sterile)

TW: "路尼耳" 眼科試驗鏡片組 (未滅菌)

Taiwan·Risk Class 1·MD·LUNEAU TECHNOLOGY OPERATIONS·Registered Apr 20, 2017 – Apr 20, 2027Active

Registration details

Analysis ID: a343877fa1c09ed330b0298bb792d2f5
License Form: Ministry of Health Medical Device Import No. 017743
Customs Code: DHA09401774308

Company information

Manufacturer: LUNEAU TECHNOLOGY OPERATIONS
Manufacturer Country: France
Authorized Representative: JUN FENG OPTICAL CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M1405 Ophthalmic Test Lens Group
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 20, 2017
Expiry Date: Apr 20, 2027

About this record

Access comprehensive regulatory information for "Luneau" 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 a343877fa1c09ed330b0298bb792d2f5 and manufactured by LUNEAU TECHNOLOGY OPERATIONS. The authorized representative in Taiwan is JUN FENG OPTICAL CO., LTD..

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