Taiwan FDA registration 8a41a07aea312ae5243e6addc4e0ae88
RenehaVis
TW: 力欣維關節內注射劑
Taiwan·Risk Class 3·MD·MDT Int’l S.A.·Registered May 21, 2019 – May 21, 2024ExpiredRegistration details
- Analysis ID
- 8a41a07aea312ae5243e6addc4e0ae88
- License Form
- Ministry of Health Medical Device Import No. 031890
- Customs Code
- DHA05603189009
Company information
- Manufacturer
- MDT Int’l S.A.
- Manufacturer Country
- Switzerland
- Authorized Representative
- HOLYLIFE BIOPHARMA CO., LTD.
Product details
- Intended Use
- Provides lubrication for patients with degenerative knee arthritis to reduce the symptoms of joint pain.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N0003 Hyaluronic acid implants for the joint cavity
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 21, 2019
- Expiry Date
- May 21, 2024
About this record
Access comprehensive regulatory information for RenehaVis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8a41a07aea312ae5243e6addc4e0ae88 and manufactured by MDT Int’l S.A.. The authorized representative in Taiwan is HOLYLIFE BIOPHARMA CO., LTD..
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