Taiwan FDA registration c08ac6ed6a5fa8bc09b37f110dcbfbfa
Opsia intraocular lens
TW: 歐普西亞人工水晶體
Registration details
- Analysis ID
- c08ac6ed6a5fa8bc09b37f110dcbfbfa
- Customs Code
- DHAS0600845000
Company information
- Manufacturer
- CHAUVIN-OPSIA LABORATORIES
- Manufacturer Country
- France
- Authorized Representative
- Zhanxin Co., Ltd
Product details
- Product Type (Level 1)
- 0300 Prosthetic function substitute
- Import Information
- import
Dates and status
- Registration Date
- Nov 18, 1997
- Expiry Date
- Nov 18, 2002
- Cancellation Date
- Dec 01, 2004
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Opsia intraocular lens in Taiwan's medical device market through Pure Global AI's free database. is registered under number c08ac6ed6a5fa8bc09b37f110dcbfbfa and manufactured by CHAUVIN-OPSIA LABORATORIES. The authorized representative in Taiwan is Zhanxin 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