Taiwan FDA registration 3cef155a263de8f237021aae8df4c12e
"Xingchang" light nasal organ
TW: “杏昌”光鼻器
Taiwan·Risk Class 2·Changzhou Biolight Medical Devices Co., Ltd.;; Biolight Medical Devices Ltd.·Registered Oct 13, 2022 – Oct 13, 2027ActiveRegistration details
- Analysis ID
- 3cef155a263de8f237021aae8df4c12e
- Customs Code
- DHA09200141402
Company information
- Manufacturer Country
- Israel;;China
- Authorized Representative
- HI-CLEARANCE 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)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Input;; Chinese goods;; Contract manufacturing
Dates and status
- Registration Date
- Oct 13, 2022
- Expiry Date
- Oct 13, 2027
About this record
Access comprehensive regulatory information for "Xingchang" light nasal organ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3cef155a263de8f237021aae8df4c12e and manufactured by Changzhou Biolight Medical Devices Co., Ltd.;; Biolight Medical Devices Ltd.. The authorized representative in Taiwan is HI-CLEARANCE INC..
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