Taiwan FDA registration 087e3f8cf42afa8a6f1e648453776566
"Pipeden" calcium hydroxide filler
TW: “派普登”氫氧化鈣充填劑
Taiwan·Risk Class 2·PULPDENT CORPORATION·Registered Mar 18, 2010 – Mar 18, 2025ExpiredRegistration details
- Analysis ID
- 087e3f8cf42afa8a6f1e648453776566
- Customs Code
- DHA00602067705
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 18, 2010
- Expiry Date
- Mar 18, 2025
- Cancellation Date
- Feb 10, 2023
About this record
Access comprehensive regulatory information for "Pipeden" calcium hydroxide filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 087e3f8cf42afa8a6f1e648453776566 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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