Taiwan FDA registration b69e0b05d0f019f521194ebd43297217
“Ivoclar Vivadent”Resin Impression Tray Material (Non-Sterile)
TW: “義獲嘉偉瓦登特”樹脂印模牙托材 (未滅菌)
Taiwan·Risk Class 1·MD·IVOCLAR VIVADENT AG·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- b69e0b05d0f019f521194ebd43297217
- License Form
- Ministry of Health Medical Device Import Registration No. 009256
- Customs Code
- DHA08400925605
Company information
- Manufacturer
- IVOCLAR VIVADENT AG
- Manufacturer Country
- Liechtenstein
- Authorized Representative
- BioLaden Consultant Corp.
Product details
- Intended Use
- Limited to the first level identification range of resin impression dental tray (F.3670) of the management method for medical equipment.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3670 resin impression dental tray
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for “Ivoclar Vivadent”Resin Impression Tray Material (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 b69e0b05d0f019f521194ebd43297217 and manufactured by IVOCLAR VIVADENT AG. The authorized representative in Taiwan is BioLaden Consultant Corp..
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