Taiwan FDA registration 76a42c615ed10c797926c1fbfa3ecc53
"Shapaulette" Fuller pulsed light
TW: “夏普萊特”馥美脈衝光
Taiwan·Risk Class 2·Sharplight Technologies Ltd·Registered Nov 03, 2016 – Nov 03, 2021CancelledRegistration details
- Analysis ID
- 76a42c615ed10c797926c1fbfa3ecc53
- Customs Code
- DHA05602901204
Company information
- Manufacturer
- Sharplight Technologies Ltd
- Manufacturer Country
- Israel
- Authorized Representative
- COLLAMATRIX CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Nov 03, 2016
- Expiry Date
- Nov 03, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Shapaulette" Fuller pulsed light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76a42c615ed10c797926c1fbfa3ecc53 and manufactured by Sharplight Technologies Ltd. The authorized representative in Taiwan is COLLAMATRIX CO., LTD..
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