Taiwan FDA registration 9efae7e04d5390ff591cecd061a5dc8f
"Meta" Gutta Percha (Non-Sterile)
TW: "美大" 馬來膠 (未滅菌)
Registration details
- Analysis ID
- 9efae7e04d5390ff591cecd061a5dc8f
- License Form
- Ministry of Health Medical Device Import No. 014753
- Customs Code
- DHA09401475309
Company information
- Manufacturer
- META BIOMED CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YONG CHIEH ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3850 Male-Glue
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2014
- Expiry Date
- Dec 16, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Meta" Gutta Percha (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 9efae7e04d5390ff591cecd061a5dc8f and manufactured by META BIOMED CO., LTD.. The authorized representative in Taiwan is YONG CHIEH ENTERPRISE 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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