Taiwan FDA registration 16efecdeb18faa0aff14c0d9e71f3a95
“Dornier” Thulio Laser Device
TW: “多尼爾”舒立歐雷射
Taiwan·Risk Class 2·MD·DORNIER MEDTECH SYSTEMS GMBH·Registered Jul 03, 2023 – Jul 03, 2028ActiveRegistration details
- Analysis ID
- 16efecdeb18faa0aff14c0d9e71f3a95
- License Form
- Ministry of Health Medical Device Import No. 036660
- Customs Code
- DHA05603666004
Company information
- Manufacturer
- DORNIER MEDTECH SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 03, 2023
- Expiry Date
- Jul 03, 2028
About this record
Access comprehensive regulatory information for “Dornier” Thulio Laser Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16efecdeb18faa0aff14c0d9e71f3a95 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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