Taiwan FDA registration 610d5fbb03702576189d4c5a565ba836

"Satelec" Oral cavity abrasive polishing agent (Non-Sterile)

TW: "賽特利"口腔研磨磨光劑 (未滅菌)

Taiwan·Risk Class 1·MD·SATELEC S.A.S. ACTEON GROUP DIVISION·Registered Sep 02, 2014 – Sep 02, 2024Expired

Registration details

Analysis ID: 610d5fbb03702576189d4c5a565ba836
License Form: Ministry of Health Medical Device Import No. 014471
Customs Code: DHA09401447102

Company information

Manufacturer: SATELEC S.A.S. ACTEON GROUP DIVISION
Manufacturer Country: France
Authorized Representative: LA FU INDUSTRIAL CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of oral grinding polishing agent (F.6030) of the management measures for medical equipment.
Product Type (Level 1): F Dental devices
Product Type (Level 2): F6030 Oral grinding polishing agent
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 02, 2014
Expiry Date: Sep 02, 2024

About this record

Access comprehensive regulatory information for "Satelec" Oral cavity abrasive polishing agent (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 610d5fbb03702576189d4c5a565ba836 and manufactured by SATELEC S.A.S. ACTEON GROUP DIVISION. The authorized representative in Taiwan is LA FU INDUSTRIAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.