Taiwan FDA registration 2d20c8ad3f99bef0daacd5e39a81ae2c
“Ditron” Dental Implant System
TW: “迪壯”骨內植體系統
Registration details
- Analysis ID
- 2d20c8ad3f99bef0daacd5e39a81ae2c
- License Form
- Ministry of Health Medical Device Import No. 030150
- Customs Code
- DHA05603015003
Company information
- Manufacturer
- Ditron Precision Ltd. Ditron Dental Division
- Manufacturer Country
- Israel
- Authorized Representative
- INETA CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3640 Bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 31, 2017
- Expiry Date
- Aug 31, 2022
About this record
Access comprehensive regulatory information for “Ditron” Dental Implant System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2d20c8ad3f99bef0daacd5e39a81ae2c and manufactured by Ditron Precision Ltd. Ditron Dental Division. The authorized representative in Taiwan is INETA CORPORATION.
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