Taiwan FDA registration 19bec248acf0f1686c7fb9c0f8ec556f

"Anxin" ophthalmic surgical glasses (magnifying glasses) (unsterilized)

TW: "安信"眼科用手術眼鏡(放大鏡)(未滅菌)

Taiwan·Risk Class 1·SHANGHAI ANXI OPTICAL EQUIPMENT MANUFACTURE CO., LTD.·Registered Aug 18, 2011 – Aug 18, 2016Cancelled

Registration details

Analysis ID: 19bec248acf0f1686c7fb9c0f8ec556f
Customs Code: DHA04600143701

Company information

Manufacturer: SHANGHAI ANXI OPTICAL EQUIPMENT MANUFACTURE CO., LTD.
Manufacturer Country: China
Authorized Representative: XIN BO ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of "Ophthalmic Surgical Glasses (Magnifying Glasses) (M.4770)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.4770 Ophthalmic surgical lenses (magnifying lenses)
Import Information: import

Dates and status

Registration Date: Aug 18, 2011
Expiry Date: Aug 18, 2016
Cancellation Date: Jun 26, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Anxin" ophthalmic surgical glasses (magnifying glasses) (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 19bec248acf0f1686c7fb9c0f8ec556f and manufactured by SHANGHAI ANXI OPTICAL EQUIPMENT MANUFACTURE CO., LTD.. The authorized representative in Taiwan is XIN BO ENTERPRISE CO., LTD..

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