Taiwan FDA registration 6f330b409912666f2650ed8b65e6b3ee
WaveLight Analyzer II
TW: “威萊特” 波前像差分析儀
Taiwan·Risk Class 2·MD·WAVELIGHT GMBH·Registered Aug 01, 2013 – Aug 01, 2023ExpiredRegistration details
- Analysis ID
- 6f330b409912666f2650ed8b65e6b3ee
- License Form
- Ministry of Health Medical Device Import No. 024610
- Customs Code
- DHA05602461002
Company information
- Manufacturer
- WAVELIGHT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1850 AC power type fine gap lamp
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 01, 2013
- Expiry Date
- Aug 01, 2023
About this record
Access comprehensive regulatory information for WaveLight Analyzer II in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f330b409912666f2650ed8b65e6b3ee and manufactured by WAVELIGHT GMBH. The authorized representative in Taiwan is ALCON SERVICES AG, TAIWAN BRANCH (SWITZERLAND).
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