Taiwan FDA registration 3fba222befea5cbe9528625f325643be
"Intermetate" laser diode
TW: “因特美地”雷射二極儀
Taiwan·Risk Class 2·INTERMEDIC ARFRAN, S.A.·Registered Aug 23, 2011 – Aug 23, 2021CancelledRegistration details
- Analysis ID
- 3fba222befea5cbe9528625f325643be
- Customs Code
- DHA00602275802
Company information
- Manufacturer
- INTERMEDIC ARFRAN, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- EVERMED INTERNATIONAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- import
Dates and status
- Registration Date
- Aug 23, 2011
- Expiry Date
- Aug 23, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Intermetate" laser diode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fba222befea5cbe9528625f325643be and manufactured by INTERMEDIC ARFRAN, S.A.. The authorized representative in Taiwan is EVERMED INTERNATIONAL CO., LTD..
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