Taiwan FDA registration 0b9f33caed75674a5076b4cbe204e9bc
"Delden" root tube paper needle (unsterilized)
TW: “岱爾登”根管紙針(未滅菌)
Taiwan·Risk Class 1·DIADENT GROUP INTERNATIONAL·Registered Jun 13, 2011 – Jun 13, 2016CancelledRegistration details
- Analysis ID
- 0b9f33caed75674a5076b4cbe204e9bc
- Customs Code
- DHA04401046902
Company information
- Manufacturer
- DIADENT GROUP INTERNATIONAL
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MODFIT ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3830 Root Canal
- Import Information
- import
Dates and status
- Registration Date
- Jun 13, 2011
- Expiry Date
- Jun 13, 2016
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Delden" root tube paper needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b9f33caed75674a5076b4cbe204e9bc and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is MODFIT ENTERPRISE CO., LTD..
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