Taiwan FDA registration e66f99d5687bafff3972ae4484c3d638
"CANON" FULL AUTO REF-KERATOMETER (Non-Sterile)
TW: "佳能" 全自動電腦驗光及角膜弧度儀(未滅菌)
Taiwan·Risk Class 1·MD·CANON COMPONENTS,INC.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- e66f99d5687bafff3972ae4484c3d638
- License Form
- Ministry of Health Medical Device Import Registration No. 000007
- Customs Code
- DHA08400000704
Company information
- Manufacturer
- CANON COMPONENTS,INC.
- Manufacturer Country
- Japan
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Measure eye refraction and corneal curvature.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1760 Ophthalmic Refractive Machine
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "CANON" FULL AUTO REF-KERATOMETER (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e66f99d5687bafff3972ae4484c3d638 and manufactured by CANON COMPONENTS,INC.. The authorized representative in Taiwan is CLINICO INC..
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