Taiwan FDA registration d16662d360b0b6ec99f41dbd3ef48475
“GANESHA & DEVICE”corrective spectacle lens(Non-sterile)
TW: “迦納夏”矯正鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·DAEMYUNG OPTICAL CO. LTD.·Registered Nov 21, 2013 – Nov 21, 2018CancelledRegistration details
- Analysis ID
- d16662d360b0b6ec99f41dbd3ef48475
- License Form
- Ministry of Health Medical Device Import No. 013618
- Customs Code
- DHA09401361801
Company information
- Manufacturer
- DAEMYUNG OPTICAL CO. LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YI JIA YI OPTICAL CO., LTD.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 21, 2013
- Expiry Date
- Nov 21, 2018
- Cancellation Date
- Aug 30, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “GANESHA & DEVICE”corrective spectacle lens(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 d16662d360b0b6ec99f41dbd3ef48475 and manufactured by DAEMYUNG OPTICAL CO. LTD.. The authorized representative in Taiwan is YI JIA YI OPTICAL CO., LTD..
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