Taiwan FDA registration 262130b28574d2a8d5854752041856ee
"Dio" Dental hand instrument (Non-sterile)
TW: "帝歐" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·DIO CORPORATION·Registered May 07, 2019 – May 07, 2024ExpiredRegistration details
- Analysis ID
- 262130b28574d2a8d5854752041856ee
- License Form
- Ministry of Health Medical Device Import No. 020419
- Customs Code
- DHA09402041909
Company information
- Manufacturer
- DIO CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
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
- May 07, 2019
- Expiry Date
- May 07, 2024
About this record
Access comprehensive regulatory information for "Dio" Dental hand instrument (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 262130b28574d2a8d5854752041856ee and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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