Taiwan FDA registration 95fa1ad7ece20315e434271933174491
"Okla" diagnostic concentrating lenses (unsterilized)
TW: “歐克拉” 診斷用聚光鏡片 (未滅菌)
Taiwan·Risk Class 1·OCULAR INSTRUMENTS, INC.·Registered Jan 13, 2011 – Jan 13, 2021CancelledRegistration details
- Analysis ID
- 95fa1ad7ece20315e434271933174491
- Customs Code
- DHA04400980209
Company information
- Manufacturer
- OCULAR INSTRUMENTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- VISIONRISE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Diagnostic Condensing Lenses (M.1380)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1380 診斷用聚光鏡片
- Import Information
- import
Dates and status
- Registration Date
- Jan 13, 2011
- Expiry Date
- Jan 13, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Okla" diagnostic concentrating lenses (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 95fa1ad7ece20315e434271933174491 and manufactured by OCULAR INSTRUMENTS, INC.. The authorized representative in Taiwan is VISIONRISE ENTERPRISE CO., LTD..
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