Taiwan FDA registration 461229b00f1b759be480a19e06dca871
"ORTHOPLI" DENTAL HAND INSTRUMENT (Non-Sterile)
TW: "歐瑟萊" 牙科手用器械 (未滅菌)
Taiwan·Risk Class 1·MD·ORTHOPLI CORPORATION·Registered Aug 11, 2017 – Aug 11, 2022ExpiredRegistration details
- Analysis ID
- 461229b00f1b759be480a19e06dca871
- License Form
- Ministry of Health Medical Device Import No. 018182
- Customs Code
- DHA09401818202
Company information
- Manufacturer
- ORTHOPLI CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- A & J BROS. TRADING CO., LTD.
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
- Aug 11, 2017
- Expiry Date
- Aug 11, 2022
About this record
Access comprehensive regulatory information for "ORTHOPLI" 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 461229b00f1b759be480a19e06dca871 and manufactured by ORTHOPLI CORPORATION. The authorized representative in Taiwan is A & J BROS. TRADING CO., LTD..
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