Taiwan FDA registration 7209270c346d80811988337ae50f71b5
Eubrix intra-articular injection
TW: 優倍力關節腔注射劑
Taiwan·Risk Class 3·FIDIA FARMACEUTICI S.P.A.·Registered Sep 28, 2010 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- 7209270c346d80811988337ae50f71b5
- Customs Code
- DHA00602149902
Company information
- Manufacturer
- FIDIA FARMACEUTICI S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- MED PHARMA CO., LTD.
Product details
- Intended Use
- Treatment of patients with degenerative knee arthritis pain is limited to conservative non-pharmacological treatments and when general analgesics (eg, Acetaminophen) are ineffective. Performance changes: As detailed in Chinese copy of the copy. (The original copy of the imitation list and label approved on October 13, 99 will be recycled and invalidated).
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Sep 28, 2010
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for Eubrix intra-articular injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7209270c346d80811988337ae50f71b5 and manufactured by FIDIA FARMACEUTICI S.P.A.. The authorized representative in Taiwan is MED PHARMA CO., LTD..
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