Taiwan FDA registration f13adb951c52e87b679e315448e7f487
“Oculus” Scheimpflug Camera
TW: “歐克路”前房分析儀
Taiwan·Risk Class 2·MD·OCULUS OPTIKGERATE GMBH·Registered Sep 02, 2016 – Sep 02, 2026ActiveRegistration details
- Analysis ID
- f13adb951c52e87b679e315448e7f487
- License Form
- Ministry of Health Medical Device Import No. 028778
- Customs Code
- DHA05602877805
Company information
- Manufacturer
- OCULUS OPTIKGERATE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE CO., LTD.
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
- Sep 02, 2016
- Expiry Date
- Sep 02, 2026
About this record
Access comprehensive regulatory information for “Oculus” Scheimpflug Camera in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f13adb951c52e87b679e315448e7f487 and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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