Taiwan FDA registration 153c57d3ef60c8819a80f9dfb48835fd
"Day Fiber" ENT fiber optic light source system
TW: "日光纖" 耳鼻喉光纖光源系統
Taiwan·Risk Class 1·SUNOPTIC TECHNOLOGIES·Registered Apr 11, 2006 – Apr 11, 2011CancelledRegistration details
- Analysis ID
- 153c57d3ef60c8819a80f9dfb48835fd
- Customs Code
- DHA04400356504
Company information
- Manufacturer
- SUNOPTIC TECHNOLOGIES
- Manufacturer Country
- United States
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4350 Ear, nose and throat optical fiber light sources and carriers
- Import Information
- import
Dates and status
- Registration Date
- Apr 11, 2006
- Expiry Date
- Apr 11, 2011
- Cancellation Date
- Oct 31, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Day Fiber" ENT fiber optic light source system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 153c57d3ef60c8819a80f9dfb48835fd and manufactured by SUNOPTIC TECHNOLOGIES. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
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