Taiwan FDA registration 4a49d6f28f6a275de580c6c8a47e9b8a
"Mani" dental root canal file (unsterilized)
TW: "瑪尼"牙科根管銼（未滅菌）
Taiwan·Risk Class 1·MANI,INC.·Registered Mar 13, 2006 – Mar 13, 2016CancelledRegistration details
- Analysis ID
- 4a49d6f28f6a275de580c6c8a47e9b8a
- Customs Code
- DHA04400289201
Company information
- Manufacturer
- MANI,INC.
- Manufacturer Country
- Japan
- Authorized Representative
- SE-US CO., LTD.
Product details
- Intended Use
- Hand dental instruments are hand-held instruments used to perform various procedures in general dentistry and oral surgery.
- 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
- Mar 13, 2006
- Expiry Date
- Mar 13, 2016
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Mani" dental root canal file (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a49d6f28f6a275de580c6c8a47e9b8a and manufactured by MANI,INC.. The authorized representative in Taiwan is SE-US CO., LTD..
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