Taiwan FDA registration c1cfb46bf89b2ba1299acb3764dcd99b
"Danish" Qili pulsed light therapy instrument
TW: “丹麥”綺麗脈衝光療儀
Taiwan·Risk Class 2·ELLIPSE A/S·Registered Nov 11, 2009 – Nov 11, 2014CancelledRegistration details
- Analysis ID
- c1cfb46bf89b2ba1299acb3764dcd99b
- Customs Code
- DHA00602030800
Company information
- Manufacturer
- ELLIPSE A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
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 11, 2009
- Expiry Date
- Nov 11, 2014
- Cancellation Date
- May 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Danish" Qili pulsed light therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1cfb46bf89b2ba1299acb3764dcd99b and manufactured by ELLIPSE A/S. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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