Taiwan FDA registration 512868726f4ea2f4f2d01005f2610cc7
Wright photopolymerization cavity bottom agent
TW: 萊特光聚合窩洞墊底劑
Taiwan·Risk Class 2·PULPDENT CORPORATION·Registered Mar 22, 2010 – Mar 22, 2025ExpiredRegistration details
- Analysis ID
- 512868726f4ea2f4f2d01005f2610cc7
- Customs Code
- DHA00602068300
Company information
- Manufacturer
- PULPDENT CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Yourun Dental Materials Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3250 氫氧化鈣窩洞襯底
- Import Information
- import
Dates and status
- Registration Date
- Mar 22, 2010
- Expiry Date
- Mar 22, 2025
- Cancellation Date
- Feb 10, 2023
About this record
Access comprehensive regulatory information for Wright photopolymerization cavity bottom agent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 512868726f4ea2f4f2d01005f2610cc7 and manufactured by PULPDENT CORPORATION. The authorized representative in Taiwan is Yourun Dental Materials Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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