Taiwan FDA registration 449dcb95434fd939d88a0761ef60bb9d
"Oculus" Keratograph (non-sterile)
TW: "歐可樂斯" 眼科角膜儀 (未滅菌)
Taiwan·Risk Class 1·MD·OCULUS OPTIKGERATE GMBH·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 449dcb95434fd939d88a0761ef60bb9d
- License Form
- Ministry of Health Medical Device Import Registration No. 004483
- Customs Code
- DHA08400448304
Company information
- Manufacturer
- OCULUS OPTIKGERATE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Oculus" Keratograph (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 449dcb95434fd939d88a0761ef60bb9d and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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