Taiwan FDA registration 8096cc6afbb8c9e4c71dd803e9d20c0e
“Asclepion” MeDioStar laser
TW: “阿斯克比恩”密迪歐星雷射儀
Taiwan·Risk Class 2·MD·Asclepion Laser Technologies GmbH·Registered Mar 21, 2021 – Mar 21, 2026ExpiredRegistration details
- Analysis ID
- 8096cc6afbb8c9e4c71dd803e9d20c0e
- License Form
- Ministry of Health Medical Device Import No. 034407
- Customs Code
- DHA05603440708
Company information
- Manufacturer
- Asclepion Laser Technologies GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
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
- Mar 21, 2021
- Expiry Date
- Mar 21, 2026
About this record
Access comprehensive regulatory information for “Asclepion” MeDioStar laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8096cc6afbb8c9e4c71dd803e9d20c0e and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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