Taiwan FDA registration f82bbf42313271c2ffdadc58de65fe68
"DyanFlex" Dental Hand Instrument (Non-Sterile)
TW: "黛娜妃"牙科手用器械(未滅菌)
Taiwan·Risk Class 1·MD·DyanFlex·Registered Jun 09, 2015 – Jun 09, 2020CancelledRegistration details
- Analysis ID
- f82bbf42313271c2ffdadc58de65fe68
- License Form
- Ministry of Health Medical Device Import No. 015320
- Customs Code
- DHA09401532009
Company information
- Manufacturer
- DyanFlex
- Manufacturer Country
- United States
- Authorized Representative
- PULLIER CO., LTD.
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 09, 2015
- Expiry Date
- Jun 09, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "DyanFlex" Dental Hand Instrument (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 f82bbf42313271c2ffdadc58de65fe68 and manufactured by DyanFlex. The authorized representative in Taiwan is PULLIER 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.
Free DatabasePowered by Pure Global AI89,000+ Devices