Taiwan FDA registration dcc331af6203005c36a070c0f476fab4
“Ivoclar Vivadent” Dental hand instrument (Non-Sterile)
TW: "義獲嘉偉瓦登特”牙科手用器械(未滅菌)
Taiwan·Risk Class 1·MD·IVOCLAR VIVADENT AG·Registered Dec 31, 2019 – Dec 31, 2024ExpiredRegistration details
- Analysis ID
- dcc331af6203005c36a070c0f476fab4
- License Form
- Ministry of Health Medical Device Import No. 021154
- Customs Code
- DHA09402115404
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
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
- Dec 31, 2019
- Expiry Date
- Dec 31, 2024
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent” 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 dcc331af6203005c36a070c0f476fab4 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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