Taiwan FDA registration 5d0d6415ceeaa738ebdbc3141b225202
“Quanta” New Q-PLUS Laser System
TW: “廣特”紐圖勒斯雷射系統
Taiwan·Risk Class 2·MD·Quanta System S.p.A·Registered Jul 28, 2014 – Jul 28, 2019CancelledRegistration details
- Analysis ID
- 5d0d6415ceeaa738ebdbc3141b225202
- License Form
- Ministry of Health Medical Device Import No. 026354
- Customs Code
- DHA05602635404
Company information
- Manufacturer
- Quanta System S.p.A
- Manufacturer Country
- Italy
- Authorized Representative
- Polytechnic Technology Engineering Consultants Limited
Product details
- 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
- Jul 28, 2014
- Expiry Date
- Jul 28, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Quanta” New Q-PLUS Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5d0d6415ceeaa738ebdbc3141b225202 and manufactured by Quanta System S.p.A. The authorized representative in Taiwan is Polytechnic Technology Engineering Consultants Limited.
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