Taiwan FDA registration 648d0d5a27fa63b1d3936a96acce6caf
"SOPRO" Radiographic film (Non-Sterile)
TW: "舒涪" 放射線影片 (未滅菌)
Taiwan·Risk Class 1·MD·SOPRO, A COMPANY OF ACTEON GROUP·Registered May 19, 2017 – May 19, 2022ExpiredRegistration details
- Analysis ID
- 648d0d5a27fa63b1d3936a96acce6caf
- License Form
- Ministry of Health Medical Device Import No. 017857
- Customs Code
- DHA09401785700
Company information
- Manufacturer
- SOPRO, A COMPANY OF ACTEON GROUP
- Manufacturer Country
- France
- Authorized Representative
- JOYO WELLDENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Radiographic Film (P.1840)".
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1840 Radiographic video
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 19, 2017
- Expiry Date
- May 19, 2022
About this record
Access comprehensive regulatory information for "SOPRO" Radiographic film (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 648d0d5a27fa63b1d3936a96acce6caf and manufactured by SOPRO, A COMPANY OF ACTEON GROUP. The authorized representative in Taiwan is JOYO WELLDENT CO., LTD..
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