Taiwan FDA registration 9f72e6e530a3643ed437587a56343c41
"FASA" Intra-Tooth Implant Manipulation Device (Inverted Bacteria)
TW: "法莎" 牙齒骨內植入物操作器材(未滅菌)
Registration details
- Analysis ID
- 9f72e6e530a3643ed437587a56343c41
- Customs Code
- DHA09402350606
Company information
- Manufacturer
- VERSAH LLC
- Manufacturer Country
- United States
- Authorized Representative
- THREE A CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Dental Intraosseous Implant Operation Equipment (F.3980)" for the classification and grading management measures of medical devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 13, 2024
- Expiry Date
- Jun 13, 2029
About this record
Access comprehensive regulatory information for "FASA" Intra-Tooth Implant Manipulation Device (Inverted Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f72e6e530a3643ed437587a56343c41 and manufactured by VERSAH LLC. The authorized representative in Taiwan is THREE A 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.
Free DatabasePowered by Pure Global AI89,000+ Devices