Taiwan FDA registration 1e5a71c1e67004a931fab0eff565024a
"Kaile" fundus lens series and accessories
TW: "凱樂"眼底鏡系列及附件
Taiwan·Risk Class 2·KEELER LTD.·Registered Jun 14, 2006 – Jun 14, 2026ExpiredRegistration details
- Analysis ID
- 1e5a71c1e67004a931fab0eff565024a
- Customs Code
- DHA00601668400
Company information
- Manufacturer
- KEELER LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TAIWAN OPTICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmology
- Import Information
- import
Dates and status
- Registration Date
- Jun 14, 2006
- Expiry Date
- Jun 14, 2026
About this record
Access comprehensive regulatory information for "Kaile" fundus lens series and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1e5a71c1e67004a931fab0eff565024a and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL CO., LTD..
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