Taiwan FDA registration 6696aab0a2c3494f83bd34abfa06e20e
"Lake" corneal mapper (unsterilized)
TW: “萊克”角膜地圖儀 (未滅菌)
Taiwan·Risk Class 1·REICHERT, INC.·Registered Jun 30, 2006 – Jun 30, 2011CancelledRegistration details
- Analysis ID
- 6696aab0a2c3494f83bd34abfa06e20e
- Customs Code
- DHA04400483502
Company information
- Manufacturer
- REICHERT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.1350 Coratoscope
- Import Information
- import
Dates and status
- Registration Date
- Jun 30, 2006
- Expiry Date
- Jun 30, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lake" corneal mapper (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6696aab0a2c3494f83bd34abfa06e20e and manufactured by REICHERT, INC.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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