Taiwan FDA registration 0e190f1a2a96e1cf7ce1aa084fc30502
"Preqing" ophthalmic keratoscope (unsterilized)
TW: “普瑞晴”眼科角膜鏡(未滅菌)
Registration details
- Analysis ID
- 0e190f1a2a96e1cf7ce1aa084fc30502
- Customs Code
- DHA04400819407
Company information
- Manufacturer
- PARADIGM MEDICAL INDUSTRIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHIU HO MEDICAL SYSTEM CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Oct 09, 2009
- Expiry Date
- Oct 09, 2014
- Cancellation Date
- Jun 14, 2010
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Preqing" ophthalmic keratoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e190f1a2a96e1cf7ce1aa084fc30502 and manufactured by PARADIGM MEDICAL INDUSTRIES, INC.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM 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