Taiwan FDA registration b9d40aa3d069a6ef4fde51c62ae7a835
"Spidon" temporary sminting (unsterilized)
TW: "司必登" 臨時士敏汀 (未滅菌)
Registration details
- Analysis ID
- b9d40aa3d069a6ef4fde51c62ae7a835
- Customs Code
- DHA04401046606
Company information
- Manufacturer
- SPIDENT CO. LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HON INTERNATIONAL TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of dental cement (Smintin) (F.3275) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3275 牙科用水泥(士敏汀)
- Import Information
- import
Dates and status
- Registration Date
- Jun 10, 2011
- Expiry Date
- Jun 10, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Spidon" temporary sminting (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b9d40aa3d069a6ef4fde51c62ae7a835 and manufactured by SPIDENT CO. LTD.. The authorized representative in Taiwan is HON INTERNATIONAL TRADING CO., LTD..
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