Taiwan FDA registration 39429e3aee0957da6e50378e068855ad
"Biodenta" Surgical Guide (Non-Sterile)
TW: "百丹特" 手術導板 (未滅菌)
Taiwan·Risk Class 1·MD·BIODENTA SWISS AG·Registered Nov 10, 2017 – Nov 10, 2027ActiveRegistration details
- Analysis ID
- 39429e3aee0957da6e50378e068855ad
- License Form
- Ministry of Health Medical Device Import No. 018486
- Customs Code
- DHA09401848606
Company information
- Manufacturer
- BIODENTA SWISS AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- Dentauspex Corporation
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 10, 2017
- Expiry Date
- Nov 10, 2027
About this record
Access comprehensive regulatory information for "Biodenta" Surgical Guide (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 39429e3aee0957da6e50378e068855ad and manufactured by BIODENTA SWISS AG. The authorized representative in Taiwan is Dentauspex 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