Taiwan FDA registration 9fdb24d90e1d69fcfc150eace96ed15b
“OLYMPUS” Evis Lucera Elite Gastrointestinalvideoscope
TW: “奧林柏斯”電子式胃鏡
Taiwan·Risk Class 2·MD·AIZU OLYMPUS CO., LTD·Registered Jan 18, 2019 – Jan 18, 2029ActiveRegistration details
- Analysis ID
- 9fdb24d90e1d69fcfc150eace96ed15b
- License Form
- Ministry of Health Medical Device Import No. 032212
- Customs Code
- DHA05603221209
Company information
- Manufacturer
- AIZU OLYMPUS CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
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
- Jan 18, 2019
- Expiry Date
- Jan 18, 2029
About this record
Access comprehensive regulatory information for “OLYMPUS” Evis Lucera Elite Gastrointestinalvideoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fdb24d90e1d69fcfc150eace96ed15b and manufactured by AIZU OLYMPUS CO., LTD. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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