Taiwan FDA registration 1448c2ceb107969305ed4dc9ba7feef8
Seff Diju Dental Implant Phase 2 Parts System
TW: 賽芙帝駒植牙第二階段零件系統
Taiwan·Risk Class 3·FRIADENT GMBH·Registered Dec 11, 2006 – Dec 11, 2016CancelledRegistration details
- Analysis ID
- 1448c2ceb107969305ed4dc9ba7feef8
- Customs Code
- DHA00601747601
Company information
- Manufacturer
- FRIADENT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- JSD International Inc
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
- Dec 11, 2006
- Expiry Date
- Dec 11, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Seff Diju Dental Implant Phase 2 Parts System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1448c2ceb107969305ed4dc9ba7feef8 and manufactured by FRIADENT GMBH. The authorized representative in Taiwan is JSD International Inc.
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