Taiwan FDA registration 57e42ae626e61bb22e92dba79d1b8521
"Oculus" Ophthalmic trial lens set (non-sterile)
TW: "歐可樂斯" 眼科試驗鏡片組 (未滅菌)
Taiwan·Risk Class 1·MD·OCULUS OPTIKGERATE GMBH·Registered Mar 24, 2017 – Mar 24, 2022ExpiredRegistration details
- Analysis ID
- 57e42ae626e61bb22e92dba79d1b8521
- License Form
- Ministry of Health Medical Device Import No. 017641
- Customs Code
- DHA09401764100
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 recognition range of the ophthalmic test lens group (M.1405) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1405 Ophthalmic Test Lens Group
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 24, 2017
- Expiry Date
- Mar 24, 2022
About this record
Access comprehensive regulatory information for "Oculus" Ophthalmic trial lens set (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 57e42ae626e61bb22e92dba79d1b8521 and manufactured by OCULUS OPTIKGERATE GMBH. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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