Taiwan FDA registration a447f2fd2a7aef1ab307573867a07ade
"Platinum" implant system (tissue type)
TW: “百丹特”人工植體系統(組織型)
Taiwan·Risk Class 3·BIODENTA SWISS AG·Registered Oct 28, 2010 – Oct 28, 2020CancelledRegistration details
- Analysis ID
- a447f2fd2a7aef1ab307573867a07ade
- Customs Code
- DHA00602160702
Company information
- Manufacturer
- BIODENTA SWISS AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- BIODENTA CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2010
- Expiry Date
- Oct 28, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Platinum" implant system (tissue type) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a447f2fd2a7aef1ab307573867a07ade and manufactured by BIODENTA SWISS AG. The authorized representative in Taiwan is BIODENTA 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