Taiwan FDA registration 0d7cff5795a1c0b0f1d4528e873f9092
“Kerr” OptiBond eXTRa Universal
TW: “科爾”歐邦艾拉自蝕黏著劑
Taiwan·Risk Class 2·MD·KERR CORPORATION·Registered Sep 17, 2020 – Sep 17, 2025ExpiredRegistration details
- Analysis ID
- 0d7cff5795a1c0b0f1d4528e873f9092
- License Form
- Ministry of Health Medical Device Import No. 033858
- Customs Code
- DHA05603385800
Company information
- Manufacturer
- KERR CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- NOBEL BIOCARE TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3200 resin dental adhesive
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 17, 2020
- Expiry Date
- Sep 17, 2025
About this record
Access comprehensive regulatory information for “Kerr” OptiBond eXTRa Universal in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d7cff5795a1c0b0f1d4528e873f9092 and manufactured by KERR CORPORATION. The authorized representative in Taiwan is NOBEL BIOCARE TAIWAN CO., LTD..
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