Taiwan FDA registration 3316225f24a0f35fd241e03ee47e8db4
Acavitta Elite Light Subcutaneous Filling Agent (with Liducaine)
TW: 艾珂薇塔菁伶輕感皮下填補劑(含利度卡因)
Taiwan·Risk Class 3·SCIVISION BIOTECH INC.·Registered Sep 10, 2024 – Apr 13, 2027ActiveRegistration details
- Analysis ID
- 3316225f24a0f35fd241e03ee47e8db4
Company information
- Manufacturer
- SCIVISION BIOTECH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SCIVISION BIOTECH 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.0007 Hyaluronic acid implants
- Import Information
- Domestic;; Security surveillance
Dates and status
- Registration Date
- Sep 10, 2024
- Expiry Date
- Apr 13, 2027
About this record
Access comprehensive regulatory information for Acavitta Elite Light Subcutaneous Filling Agent (with Liducaine) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3316225f24a0f35fd241e03ee47e8db4 and manufactured by SCIVISION BIOTECH INC.. The authorized representative in Taiwan is SCIVISION BIOTECH INC..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices