Taiwan FDA registration f45e3497bb4eadae6db5298360bff27c
“HONHI” Gutta Percha (Non-Sterile)
TW: “鴻海”馬來膠 (未滅菌)
Taiwan·Risk Class 1·MD·PEARL DENT CO., LTD·Registered Jan 09, 2015 – Jan 09, 2020CancelledRegistration details
- Analysis ID
- f45e3497bb4eadae6db5298360bff27c
- License Form
- Ministry of Health Medical Device Import No. 014835
- Customs Code
- DHA09401483501
Company information
- Manufacturer
- PEARL DENT CO., LTD
- Manufacturer Country
- Viet Nam
- Authorized Representative
- HONHI MEDICAL 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
- Jan 09, 2015
- Expiry Date
- Jan 09, 2020
- 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 “HONHI” 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 f45e3497bb4eadae6db5298360bff27c and manufactured by PEARL DENT CO., LTD. The authorized representative in Taiwan is HONHI MEDICAL CO., LTD..
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