Taiwan FDA registration 9dd3f357a21f9832d5e1b03cc813d32b
"McLovever" Gidis root tube paper needle (unsterilized)
TW: “麥樂佛”吉帝斯根管紙針（未滅菌）
Taiwan·Risk Class 1·MAILLEFER INSTRUMENTS HOLDING·Registered Apr 17, 2009 – Apr 17, 2019CancelledRegistration details
- Analysis ID
- 9dd3f357a21f9832d5e1b03cc813d32b
- Customs Code
- DHAS4400764708
Company information
- Manufacturer
- MAILLEFER INSTRUMENTS HOLDING
- Manufacturer Country
- Switzerland
- Authorized Representative
- Taiwan Branch of American Denspie 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
- Apr 17, 2009
- Expiry Date
- Apr 17, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "McLovever" Gidis 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 9dd3f357a21f9832d5e1b03cc813d32b and manufactured by MAILLEFER INSTRUMENTS HOLDING. The authorized representative in Taiwan is Taiwan Branch of American Denspie Co., Ltd.
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