Taiwan FDA registration 7dff266449f01834257c7890cc7ea65d

"MDT" Spectacle dissociation test system (Non-Sterile)

TW: "恩地特" 視覺分離試驗系統

Taiwan·Risk Class 1·MD·MDT sp. z o.o.·Registered Nov 09, 2022 – Nov 09, 2027Active

Registration details

Analysis ID: 7dff266449f01834257c7890cc7ea65d
License Form: Ministry of Health Medical Device Import No. 022948
Customs Code: DHA09402294807

Company information

Manufacturer: MDT sp. z o.o.
Manufacturer Country: Poland
Authorized Representative: TAIWAN OPTICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Visual Separation Test System (M.1910)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M1910 Visual Separation Test System
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 09, 2022
Expiry Date: Nov 09, 2027

About this record

Access comprehensive regulatory information for "MDT" Spectacle dissociation test system (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 7dff266449f01834257c7890cc7ea65d and manufactured by MDT sp. z o.o.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..

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