Taiwan FDA registration 3ec59df542e05a3005e673a3c1933b8c
“Hiossen” ET SA Implant System
TW: “海爾森”醫特牙科植體系統
Taiwan·Risk Class 3·MD·HIOSSEN INC.·Registered Apr 14, 2022 – Apr 14, 2027ActiveRegistration details
- Analysis ID
- 3ec59df542e05a3005e673a3c1933b8c
- License Form
- Ministry of Health Medical Device Import No. 035382
- Customs Code
- DHA05603538200
Company information
- Manufacturer
- HIOSSEN INC.
- Manufacturer Country
- United States
- Authorized Representative
- OSSTEM CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3640 Bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 14, 2022
- Expiry Date
- Apr 14, 2027
About this record
Access comprehensive regulatory information for “Hiossen” ET SA 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 3ec59df542e05a3005e673a3c1933b8c and manufactured by HIOSSEN INC.. The authorized representative in Taiwan is OSSTEM 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