Taiwan FDA registration 2eec97fa576ba12692e3ff7ddc0ab8d9
“Asclepion” Dermablate Er:YAG Laser
TW: “阿斯克比恩”鉺雅鉻皮膚雷射儀
Taiwan·Risk Class 2·MD·Asclepion Laser Technologies GmbH·Registered Jun 16, 2014 – Jun 16, 2024ExpiredRegistration details
- Analysis ID
- 2eec97fa576ba12692e3ff7ddc0ab8d9
- License Form
- Ministry of Health Medical Device Import No. 026311
- Customs Code
- DHA05602631102
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
- Jun 16, 2014
- Expiry Date
- Jun 16, 2024
About this record
Access comprehensive regulatory information for “Asclepion” Dermablate Er:YAG Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2eec97fa576ba12692e3ff7ddc0ab8d9 and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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