Taiwan FDA registration f07fcfca0a7e185ec6114cb18fa54272
"Jean" Isis Nysis Sight Glass (Unsterilized)
TW: “吉恩”艾希斯眼振觀察鏡 (未滅菌)
Taiwan·Risk Class 1·GN OTOMETRICS A/S·Registered Jun 07, 2013 – Jun 07, 2018CancelledRegistration details
- Analysis ID
- f07fcfca0a7e185ec6114cb18fa54272
- Customs Code
- DHA04401309206
Company information
- Manufacturer
- GN OTOMETRICS A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- FORMOSA MEDICAL INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Temperature or Water Temperature Difference Test Stimulator (G.1800)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.1800 Atmospheric or Water Temperature Differential Stimulation Device
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jun 07, 2013
- Expiry Date
- Jun 07, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Jean" Isis Nysis Sight Glass (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f07fcfca0a7e185ec6114cb18fa54272 and manufactured by GN OTOMETRICS A/S. The authorized representative in Taiwan is FORMOSA MEDICAL INSTRUMENTS 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