Taiwan FDA registration 9d88c17c62dfc5292855a019515391ef
“OLYMPUS” Single Use Guiding Device
TW: “奧林柏斯”單次使用導引裝置
Taiwan·Risk Class 2·MD·AOMORI OLYMPUS CO., LTD.·Registered Jul 31, 2017 – Jul 31, 2027ActiveRegistration details
- Analysis ID
- 9d88c17c62dfc5292855a019515391ef
- License Form
- Ministry of Health Medical Device Import No. 030038
- Customs Code
- DHA05603003809
Company information
- Manufacturer
- AOMORI 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
- Jul 31, 2017
- Expiry Date
- Jul 31, 2027
About this record
Access comprehensive regulatory information for “OLYMPUS” Single Use Guiding Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9d88c17c62dfc5292855a019515391ef and manufactured by AOMORI OLYMPUS CO., LTD.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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