Taiwan FDA registration a6b305884a147dd02a62ea434f1d9b9f
"VOROTEK" Magnifying Loupes and Accessories (Non-Sterile)
TW: "維沃塔克" 放大鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·VOROTEK PTY LTD·Registered Dec 15, 2017 – Dec 15, 2022ExpiredRegistration details
- Analysis ID
- a6b305884a147dd02a62ea434f1d9b9f
- License Form
- Ministry of Health Medical Device Import No. 018611
- Customs Code
- DHA09401861109
Company information
- Manufacturer
- VOROTEK PTY LTD
- Manufacturer Country
- Australia
- Authorized Representative
- BOYANG MEDICAL TECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 15, 2017
- Expiry Date
- Dec 15, 2022
About this record
Access comprehensive regulatory information for "VOROTEK" Magnifying Loupes and Accessories (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 a6b305884a147dd02a62ea434f1d9b9f and manufactured by VOROTEK PTY LTD. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.
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