Taiwan FDA registration 62e0b84c2e62dc9f67c835783a53472a
"Zeiss" Laura extends the focal hydrophilic posterior chamber intraocular lens
TW: “蔡司”蘿拉延伸焦段親水性後房人工水晶體
Taiwan·Risk Class 3·CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG·Registered Sep 09, 2020 – Sep 09, 2025ExpiredRegistration details
- Analysis ID
- 62e0b84c2e62dc9f67c835783a53472a
- Customs Code
- DHA05603394403
Company information
- Manufacturer
- CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG
- Manufacturer Country
- Germany
- Authorized Representative
- Carl Zeiss Co., Ltd. Taipei Branch
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.3600 Artificial Crystal
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Sep 09, 2020
- Expiry Date
- Sep 09, 2025
About this record
Access comprehensive regulatory information for "Zeiss" Laura extends the focal hydrophilic posterior chamber intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 62e0b84c2e62dc9f67c835783a53472a and manufactured by CARL ZEISS MEDITEC AG;; Carl Zeiss Meditec AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.
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