Taiwan FDA registration 57f702d31f20308e65881fe60592dc7f
"Cuisley" Vanlight battery irradiator lamp (unsterilized)
TW: “萃斯雷”凡萊特電池式照射燈 (未滅菌)
Taiwan·Risk Class 1·TRANSLITE·Registered Sep 26, 2006 – Sep 26, 2016CancelledRegistration details
- Analysis ID
- 57f702d31f20308e65881fe60592dc7f
- Customs Code
- DHA04400519902
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 "Translucent Apparatus (M.1945)".
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1945 Transilluminator
- Import Information
- import
Dates and status
- Registration Date
- Sep 26, 2006
- Expiry Date
- Sep 26, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Cuisley" Vanlight battery irradiator lamp (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 57f702d31f20308e65881fe60592dc7f and manufactured by TRANSLITE. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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