Taiwan FDA registration 095fb6eb7dcc3e861f17967725ab6194
"Aisoros" ENT fiber optic light source and vehicle (unsterilized)
TW: “艾索羅斯”耳鼻喉光纖光源及載具 (未滅菌)
Taiwan·Risk Class 1·ISOLUX LLC·Registered Feb 05, 2007 – Feb 05, 2012CancelledRegistration details
- Analysis ID
- 095fb6eb7dcc3e861f17967725ab6194
- Customs Code
- DHA04400558701
Company information
- Manufacturer
- ISOLUX LLC
- Manufacturer Country
- United States
- Authorized Representative
- PLOVER MEDICAL INSTRUMENTS, INC.
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
- Feb 05, 2007
- Expiry Date
- Feb 05, 2012
- Cancellation Date
- Apr 09, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aisoros" ENT fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 095fb6eb7dcc3e861f17967725ab6194 and manufactured by ISOLUX LLC. The authorized representative in Taiwan is PLOVER MEDICAL INSTRUMENTS, INC..
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