Taiwan FDA registration 54e8cc5158ce92a72d662926661efbbe
FreshKon Daily Contact Lens
TW: 菲士康極漾透明日拋隱形眼鏡
Taiwan·Risk Class 2·MD·Oculus Private Limited·Registered Jun 11, 2020 – May 10, 2028ActiveRegistration details
- Analysis ID
- 54e8cc5158ce92a72d662926661efbbe
- License Form
- Ministry of Health Medical Device Import No. 033760
- Customs Code
- DHA05603376006
Company information
- Manufacturer
- Oculus Private Limited
- Manufacturer Country
- Singapore
- Authorized Representative
- OCULUS CONTACT LENS 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)
- M5925 Flexible Contact Lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 11, 2020
- Expiry Date
- May 10, 2028
About this record
Access comprehensive regulatory information for FreshKon Daily Contact Lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54e8cc5158ce92a72d662926661efbbe and manufactured by Oculus Private Limited. The authorized representative in Taiwan is OCULUS CONTACT LENS CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices