Taiwan FDA registration 232e0d5323a28cd9d3eee3a5f33a5e23
"Ocular" Diagnostic condensing lens (Non-Sterile)
TW: "歐克爾"診斷用聚光鏡片 (未滅菌)
Taiwan·Risk Class 1·MD·OCULAR INSTRUMENTS, INC.·Registered Nov 09, 2017 – Nov 09, 2027ActiveRegistration details
- Analysis ID
- 232e0d5323a28cd9d3eee3a5f33a5e23
- License Form
- Ministry of Health Medical Device Import No. 018482
- Customs Code
- DHA09401848201
Company information
- Manufacturer
- OCULAR INSTRUMENTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CLINICO INC.
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 Ophthalmic devices
- Product Type (Level 2)
- M1380 Diagnostic Condensing Lens
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 09, 2017
- Expiry Date
- Nov 09, 2027
About this record
Access comprehensive regulatory information for "Ocular" Diagnostic condensing 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 232e0d5323a28cd9d3eee3a5f33a5e23 and manufactured by OCULAR INSTRUMENTS, INC.. The authorized representative in Taiwan is CLINICO INC..
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