Taiwan FDA registration 1c87369be22e6c91bf0b044afce0f4e3
“Ellipse A/S” Intense Pulsed Light System
TW: “丹麥”愛爾脈衝光系統
Taiwan·Risk Class 2·MD·ELLIPSE A/S·Registered Oct 10, 2013 – Oct 10, 2023ExpiredRegistration details
- Analysis ID
- 1c87369be22e6c91bf0b044afce0f4e3
- License Form
- Ministry of Health Medical Device Import No. 025497
- Customs Code
- DHA05602549708
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 and plastic surgical devices
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 10, 2013
- Expiry Date
- Oct 10, 2023
About this record
Access comprehensive regulatory information for “Ellipse A/S” Intense Pulsed Light System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c87369be22e6c91bf0b044afce0f4e3 and manufactured by ELLIPSE A/S. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..
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