Taiwan FDA registration 991ddc91374f5734905721a33c13f47e
"MANI" Plup Canal Files (Non-Sterile)
TW: "馬尼" 根管銼 (未滅菌)
Taiwan·Risk Class 1·MD·MANI, INC.·Registered Jun 15, 2016 – Jun 15, 2021ExpiredRegistration details
- Analysis ID
- 991ddc91374f5734905721a33c13f47e
- License Form
- Ministry of Health Medical Device Import No. 016652
- Customs Code
- DHA09401665200
Company information
- Manufacturer
- MANI, INC.
- Manufacturer Country
- Japan
- Authorized Representative
- ROLENCE ENTERPRISE INC.
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
- Jun 15, 2016
- Expiry Date
- Jun 15, 2021
About this record
Access comprehensive regulatory information for "MANI" Plup Canal Files (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 991ddc91374f5734905721a33c13f47e and manufactured by MANI, INC.. The authorized representative in Taiwan is ROLENCE ENTERPRISE INC..
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