Taiwan FDA registration 116e0c70ca50f6ea64bc3c1a35ef948c
"FCI" Ptosis Curtch (Non-Sterile)
TW: "佛朗惜眼" 上眼瞼下垂支持器 (未滅菌)
Taiwan·Risk Class 1·MD·FCI SAS·Registered Aug 11, 2015 – Aug 11, 2020CancelledRegistration details
- Analysis ID
- 116e0c70ca50f6ea64bc3c1a35ef948c
- License Form
- Ministry of Health Medical Device Import No. 015569
- Customs Code
- DHA09401556908
Company information
- Manufacturer
- FCI SAS
- Manufacturer Country
- France
- Authorized Representative
- HEALTH CARE MEDICAL INC.
Product details
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5600 Upper Eyelid Drosis Supporter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 11, 2015
- Expiry Date
- Aug 11, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "FCI" Ptosis Curtch (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 116e0c70ca50f6ea64bc3c1a35ef948c and manufactured by FCI SAS. The authorized representative in Taiwan is HEALTH CARE MEDICAL INC..
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