Taiwan FDA registration 32f75225149346b7259992f2986a17b3
"Mauna Kea" fiber optic confocal endoscopic imaging system
TW: “莫納克亞”光纖共聚焦內視鏡影像系統
Taiwan·Risk Class 2·MAUNA KEA TECHNOLOGIES·Registered Oct 21, 2010 – Oct 21, 2015CancelledRegistration details
- Analysis ID
- 32f75225149346b7259992f2986a17b3
- Customs Code
- DHA00602158801
Company information
- Manufacturer
- MAUNA KEA TECHNOLOGIES
- Manufacturer Country
- France
- Authorized Representative
- KINGDOM EAST ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Oct 21, 2010
- Expiry Date
- Oct 21, 2015
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Mauna Kea" fiber optic confocal endoscopic imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 32f75225149346b7259992f2986a17b3 and manufactured by MAUNA KEA TECHNOLOGIES. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., LTD..
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