Taiwan FDA registration 9fe9368b4786eb0810b5f687d2d7246c
“OLYMPUS” Visera Elite II Xenon Light Source
TW: “奧林柏斯”內視鏡用光源裝置及附件
Taiwan·Risk Class 2·MD·SHIRAKAWA OLYMPUS CO., LTD.·Registered Mar 30, 2018 – Mar 30, 2028ActiveRegistration details
- Analysis ID
- 9fe9368b4786eb0810b5f687d2d7246c
- License Form
- Ministry of Health Medical Device Import No. 031009
- Customs Code
- DHA05603100907
Company information
- Manufacturer
- SHIRAKAWA 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
- Mar 30, 2018
- Expiry Date
- Mar 30, 2028
About this record
Access comprehensive regulatory information for “OLYMPUS” Visera Elite II Xenon Light Source in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fe9368b4786eb0810b5f687d2d7246c and manufactured by SHIRAKAWA OLYMPUS CO., LTD.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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