Taiwan FDA registration 0f2a6e429bf99aa4ff96f3558f5cd08f
"Intermedi" Andu laser diode
TW: “因特美地”安度雷射二極儀
Taiwan·Risk Class 2·INTERMEDIC ARFRAN, S.A.·Registered Nov 09, 2011 – Nov 09, 2016CancelledRegistration details
- Analysis ID
- 0f2a6e429bf99aa4ff96f3558f5cd08f
- Customs Code
- DHA00602300408
Company information
- Manufacturer
- INTERMEDIC ARFRAN, S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- Yifeng International Enterprises Limited
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
- Nov 09, 2011
- Expiry Date
- Nov 09, 2016
- Cancellation Date
- Mar 14, 2016
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Intermedi" Andu 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 0f2a6e429bf99aa4ff96f3558f5cd08f and manufactured by INTERMEDIC ARFRAN, S.A.. The authorized representative in Taiwan is Yifeng International Enterprises Limited.
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