Taiwan FDA registration d8bc69255ff96ebbe9d7621dac3a9c51
Hyde Misty subcutaneous filler
TW: 海德密絲媚絲皮下填補劑
Registration details
- Analysis ID
- d8bc69255ff96ebbe9d7621dac3a9c51
Company information
- Manufacturer
- SCIVISION BIOTECH INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SCIVISION BIOTECH INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.0007 Hyaluronic acid implants
- Import Information
- Security Surveillance;; Domestic
Dates and status
- Registration Date
- Sep 15, 2019
- Expiry Date
- Sep 15, 2029
About this record
Access comprehensive regulatory information for Hyde Misty subcutaneous filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d8bc69255ff96ebbe9d7621dac3a9c51 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