Taiwan FDA registration 6fc20a002991a2c3635251a0ae13e7b2
"Lake" tonometer / corneal thickness measuring instrument
TW: “萊克”眼壓計/角膜厚度測量儀
Taiwan·Risk Class 2·REICHERT, INC.·Registered May 03, 2007 – May 03, 2017CancelledRegistration details
- Analysis ID
- 6fc20a002991a2c3635251a0ae13e7b2
- Customs Code
- DHA00601805301
Company information
- Manufacturer
- REICHERT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1560 超音波回音影像系統
- Import Information
- import
Dates and status
- Registration Date
- May 03, 2007
- Expiry Date
- May 03, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Lake" tonometer / corneal thickness measuring instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6fc20a002991a2c3635251a0ae13e7b2 and manufactured by REICHERT, INC.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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