Taiwan FDA registration 6fc91789f9c8229f5c6d9f3107ed624a
"DXM" Guttapercha Obturation Device (Non-sterile)
TW: "帝斯恩"根管熱充填裝置(未滅菌)
Taiwan·Risk Class 1·MD·DXM CO., LTD.·Registered Aug 19, 2014 – Aug 19, 2024ExpiredRegistration details
- Analysis ID
- 6fc91789f9c8229f5c6d9f3107ed624a
- License Form
- Ministry of Health Medical Device Import No. 014440
- Customs Code
- DHA09401444001
Company information
- Manufacturer
- DXM CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HONG HOW ENTERPRISE CO.
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 Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 19, 2014
- Expiry Date
- Aug 19, 2024
About this record
Access comprehensive regulatory information for "DXM" Guttapercha Obturation Device (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 6fc91789f9c8229f5c6d9f3107ed624a and manufactured by DXM CO., LTD.. The authorized representative in Taiwan is HONG HOW ENTERPRISE CO..
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