Taiwan FDA registration 0a04422e6111c72856979a85d41787dd
"J. Morita" Dentaport Root ZX Module (non-Sterile)
TW: "日本森田" 根管長度測量儀(未滅菌)
Taiwan·Risk Class 1·MD·J. MORITA MFG. CORP.·Registered May 24, 2018 – May 24, 2028ActiveRegistration details
- Analysis ID
- 0a04422e6111c72856979a85d41787dd
- License Form
- Ministry of Health Medical Device Import No. 019090
- Customs Code
- DHA09401909002
Company information
- Manufacturer
- J. MORITA MFG. CORP.
- Manufacturer Country
- Japan
- Authorized Representative
- FOMED BIOTECH INC.
Product details
- Intended Use
- Limited to the first level identification range of dental surgical devices and their accessories (F.6640) under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6640 Dental Surgical Devices and Their Accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 24, 2018
- Expiry Date
- May 24, 2028
About this record
Access comprehensive regulatory information for "J. Morita" Dentaport Root ZX Module (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 0a04422e6111c72856979a85d41787dd and manufactured by J. MORITA MFG. CORP.. The authorized representative in Taiwan is FOMED BIOTECH INC..
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