Taiwan FDA registration 3647f551e8382ae6b269a874a76251ec

"DynaFlex" Orthodontic appliance and accessories (Non-sterile)

TW: "黛娜妃" 牙科矯正裝置及其附件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DANYFLEX·Registered Apr 21, 2015 – Apr 21, 2020Cancelled
Registration details
Analysis ID
3647f551e8382ae6b269a874a76251ec
License Form
Ministry of Health Medical Device Import No. 015134
Customs Code
DHA09401513402
Company information
Manufacturer
DANYFLEX
Manufacturer Country
United States
Authorized Representative
PULLIER CO., LTD.
Product details
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F5410 Dental Orthodontic Devices and Their Accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 21, 2015
Expiry Date
Apr 21, 2020
Cancellation Date
Aug 05, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "DynaFlex" Orthodontic appliance and accessories (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 3647f551e8382ae6b269a874a76251ec and manufactured by DANYFLEX. The authorized representative in Taiwan is PULLIER CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including DYNAFLEX, INC., DYNAFLEX, and 3 recent registrations in the same category. 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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