Taiwan FDA registration e100ea14eee6eea0a4319da689b67a80
"Dinah Flex" dental orthodontic devices and their accessories (unsterilized)
TW: "黛娜飛克斯" 牙科矯正裝置及其附件 (未滅菌)
Registration details
- Analysis ID
- e100ea14eee6eea0a4319da689b67a80
- Customs Code
- DHA04401098109
Company information
- Manufacturer
- DYNAFLEX CO.
- Manufacturer Country
- United States
- Authorized Representative
- BIO-RAY BIOTECH INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Orthodontic Devices and Their Accessories (F.5410)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.5410 Dental orthodox equipment and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2011
- Expiry Date
- Oct 27, 2016
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dinah Flex" dental orthodontic devices and their accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e100ea14eee6eea0a4319da689b67a80 and manufactured by DYNAFLEX CO.. The authorized representative in Taiwan is BIO-RAY BIOTECH INSTRUMENT CO., LTD..
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