Taiwan FDA registration e7bb6a8fe7dfaf5018013bfc4f2bd5da
"Digeou" biostimulated swallowing therapy device
TW: “帝傑歐”維生電刺激吞嚥治療儀
Taiwan·Risk Class 2·DJO, LLC;; DJ Orthopedics de México, S.A. de C.V.·Registered Nov 11, 2011 – Nov 11, 2026ActiveRegistration details
- Analysis ID
- e7bb6a8fe7dfaf5018013bfc4f2bd5da
- Customs Code
- DHA00602292202
Company information
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- CONTINUOUS INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Nov 11, 2011
- Expiry Date
- Nov 11, 2026
About this record
Access comprehensive regulatory information for "Digeou" biostimulated swallowing therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7bb6a8fe7dfaf5018013bfc4f2bd5da and manufactured by DJO, LLC;; DJ Orthopedics de México, S.A. de C.V.. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT 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