Taiwan FDA registration 3c7b5bf796f978e4e2f20ebe1b56959b
“Sciton” BBLs System
TW: “賽頓”吉爾寬頻光照系統
Taiwan·Risk Class 2·MD·SCITON, INC.·Registered Mar 12, 2015 – Mar 12, 2020CancelledRegistration details
- Analysis ID
- 3c7b5bf796f978e4e2f20ebe1b56959b
- License Form
- Ministry of Health Medical Device Import No. 027133
- Customs Code
- DHA05602713306
Company information
- Manufacturer
- SCITON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- AESOLUTION BIOMEDICAL CO. LTD.
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
- Mar 12, 2015
- Expiry Date
- Mar 12, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for “Sciton” BBLs System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3c7b5bf796f978e4e2f20ebe1b56959b and manufactured by SCITON, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
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