Taiwan FDA registration 7e76f9636d4fdb9d9e55351474fb9d1a
HYAJOINT Synovial Fluid Supplement
TW: “科妍”海捷特關節腔注射劑
Taiwan·Risk Class 3·MD·SCIVISION BIOTECH INC.·Registered Oct 20, 2022 – Oct 20, 2027ActiveRegistration details
- Analysis ID
- 7e76f9636d4fdb9d9e55351474fb9d1a
- License Form
- Ministry of Health Medical Device Manufacturing No. 007544
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)
- N Orthopedics
- Product Type (Level 2)
- N0003 Hyaluronic acid implants for the joint cavity
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 20, 2022
- Expiry Date
- Oct 20, 2027
About this record
Access comprehensive regulatory information for HYAJOINT Synovial Fluid Supplement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7e76f9636d4fdb9d9e55351474fb9d1a and manufactured by SCIVISION BIOTECH INC.. The authorized representative in Taiwan is SCIVISION BIOTECH INC..
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