Taiwan FDA registration e5852873ea71a641054b7aed7d6bed30
Spiten root tube expansion (unsterilized)
TW: "司必登"根管擴大材(未滅菌)
Registration details
- Analysis ID
- e5852873ea71a641054b7aed7d6bed30
- Customs Code
- DHA04401046007
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 scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- Jun 09, 2011
- Expiry Date
- Jun 09, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Spiten root tube expansion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e5852873ea71a641054b7aed7d6bed30 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.
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