Taiwan FDA registration 5e43ab097dd4bd23519d0f5037ed53c7
"Pentron" Intraoral dental drill (Non-Sterile)
TW: "班特朗" 口內牙鑽頭 (未滅菌)
Taiwan·Risk Class 1·MD·PENTRON CLINICAL·Registered Aug 03, 2016 – Aug 03, 2026ActiveRegistration details
- Analysis ID
- 5e43ab097dd4bd23519d0f5037ed53c7
- License Form
- Ministry of Health Medical Device Import No. 016859
- Customs Code
- DHA09401685909
Company information
- Manufacturer
- PENTRON CLINICAL
- Manufacturer Country
- United States
- Authorized Representative
- MONITEX INDUSTRIAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of intraoral tooth drill bits (F.4130) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4130 Drill bit for internal teeth
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 03, 2016
- Expiry Date
- Aug 03, 2026
About this record
Access comprehensive regulatory information for "Pentron" Intraoral dental drill (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 5e43ab097dd4bd23519d0f5037ed53c7 and manufactured by PENTRON CLINICAL. The authorized representative in Taiwan is MONITEX INDUSTRIAL CO., LTD..
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