Taiwan FDA registration 2cb8c1ce7b5ed0d9c7186783ed1e9621
"Cuisley" fiber optic light source and vehicle (unsterilized)
TW: “萃斯雷”光纖光源及載具(未滅菌)
Taiwan·Risk Class 1·TRANSLITE·Registered Dec 21, 2007 – Dec 21, 2012CancelledRegistration details
- Analysis ID
- 2cb8c1ce7b5ed0d9c7186783ed1e9621
- Customs Code
- DHA04400641003
Company information
- Manufacturer
- TRANSLITE
- Manufacturer Country
- United States
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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
- Dec 21, 2007
- Expiry Date
- Dec 21, 2012
- Cancellation Date
- Apr 15, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cuisley" 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 2cb8c1ce7b5ed0d9c7186783ed1e9621 and manufactured by TRANSLITE. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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