Taiwan FDA registration 170e03a1dedf064b7020391954151982
"Salovey" Sharlock pulsed light system
TW: “莎洛維”莎洛克爾脈衝光系統
Taiwan·Risk Class 2·THERAVANT CORPORATION;; RH USA Inc.·Registered Aug 22, 2012 – Aug 22, 2022CancelledRegistration details
- Analysis ID
- 170e03a1dedf064b7020391954151982
- Customs Code
- DHA00602388603
Company information
- Manufacturer
- THERAVANT CORPORATION;; RH USA Inc.
- Manufacturer Country
- United States
- Authorized Representative
- G INNINGS MEDICAL 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;; Contract manufacturing
Dates and status
- Registration Date
- Aug 22, 2012
- Expiry Date
- Aug 22, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Salovey" Sharlock pulsed light system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 170e03a1dedf064b7020391954151982 and manufactured by THERAVANT CORPORATION;; RH USA Inc.. The authorized representative in Taiwan is G INNINGS MEDICAL LTD.
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