Taiwan FDA registration f7ae599f8403f9d7aa8349f3ec4fec13

"Burt" Vision Examiner (Non-sterilized)

TW: "伯特" 視力檢查儀 (未滅菌)

Taiwan·Risk Class 1·POTEC Co., Ltd.·Registered Oct 08, 2024 – Oct 08, 2029Active

Registration details

Analysis ID: f7ae599f8403f9d7aa8349f3ec4fec13
Customs Code: DHA09402362501

Company information

Manufacturer: POTEC Co., Ltd.
Manufacturer Country: Korea, Republic of
Authorized Representative: EVERLIGHT INSTRUMENT CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "Ophthalmic Projector (M.1680)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.1680 眼科用投影機
Import Information: import

Dates and status

Registration Date: Oct 08, 2024
Expiry Date: Oct 08, 2029

About this record

Access comprehensive regulatory information for "Burt" Vision Examiner (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7ae599f8403f9d7aa8349f3ec4fec13 and manufactured by POTEC Co., Ltd.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

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