“Sciton” Joule System
Taiwan·Risk Class 2·MD·SCITON, INC.·Registered Jun 16, 2015 – Jun 16, 2020Cancelled- Analysis ID
- b3fcb6ef8e2170f62fc5439e8249e82d
- License Form
- Ministry of Health Medical Device Import No. 027473
- Customs Code
- DHA05602747304
- Manufacturer
- SCITON, INC.
- Manufacturer Country
- United States
- Authorized Representative
- AESOLUTION BIOMEDICAL CO. LTD.
- 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
- Registration Date
- Jun 16, 2015
- Expiry Date
- Jun 16, 2020
- Cancellation Date
- Jun 16, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
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Access comprehensive regulatory information for “Sciton” Joule System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b3fcb6ef8e2170f62fc5439e8249e82d and manufactured by SCITON, INC.. The authorized representative in Taiwan is AESOLUTION BIOMEDICAL CO. LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SCITON, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.