Taiwan FDA registration 335d7f6fdb97856ad09a03340e2ad282
"Jiesheng" wound phototherapy instrument
TW: “捷盛”傷口光療儀
Taiwan·Risk Class 2·JSC Medical Optoelectronics Co., Ltd.;; Gateway Technologies Inc·Registered Oct 21, 2008 – Aug 26, 2023CancelledRegistration details
- Analysis ID
- 335d7f6fdb97856ad09a03340e2ad282
- Customs Code
- DHY00500253801
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JETTS BIO-PHOTON CORPORATION
Product details
- Intended Use
- To promote wound healing, this product should be prescribed by a physician.
- 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
- Domestic
Dates and status
- Registration Date
- Oct 21, 2008
- Expiry Date
- Aug 26, 2023
- Cancellation Date
- Mar 19, 2024
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Jiesheng" wound phototherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 335d7f6fdb97856ad09a03340e2ad282 and manufactured by JSC Medical Optoelectronics Co., Ltd.;; Gateway Technologies Inc. The authorized representative in Taiwan is JETTS BIO-PHOTON CORPORATION.
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