Taiwan FDA registration 494fa65d1a1084bd56d66960b3564e3e
“Mauna Kea” Fibered confocal Microscopic cellvizio system
TW: “莫納奇”光纖共聚焦內視鏡影像系統
Taiwan·Risk Class 2·MD·MAUNA KEA TECHNOLOGIES·Registered Jul 21, 2016 – Jul 21, 2026ExpiredRegistration details
- Analysis ID
- 494fa65d1a1084bd56d66960b3564e3e
- License Form
- Ministry of Health Medical Device Import No. 028694
- Customs Code
- DHA05602869402
Company information
- Manufacturer
- MAUNA KEA TECHNOLOGIES
- Manufacturer Country
- France
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 21, 2016
- Expiry Date
- Jul 21, 2026
About this record
Access comprehensive regulatory information for “Mauna Kea” Fibered confocal Microscopic cellvizio system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 494fa65d1a1084bd56d66960b3564e3e and manufactured by MAUNA KEA TECHNOLOGIES. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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