Taiwan FDA registration c246e2b7f3459476886001f99d83f4d8
“ALMA” Harmony XL PRO System
TW: “愛瑪”瀚墨霓雷射光電系統
Taiwan·Risk Class 2·MD·Alma Lasers Ltd.·Registered Aug 03, 2017 – Aug 03, 2027ActiveRegistration details
- Analysis ID
- c246e2b7f3459476886001f99d83f4d8
- License Form
- Ministry of Health Medical Device Import No. 030043
- Customs Code
- DHA05603004302
Company information
- Manufacturer
- Alma Lasers Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- NEOASIA LTD.
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; Contract manufacturing;; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
Dates and status
- Registration Date
- Aug 03, 2017
- Expiry Date
- Aug 03, 2027
About this record
Access comprehensive regulatory information for “ALMA” Harmony XL PRO System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c246e2b7f3459476886001f99d83f4d8 and manufactured by Alma Lasers Ltd.. The authorized representative in Taiwan is NEOASIA LTD..
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