Taiwan FDA registration 913b792d874769ec32dee07fbe3979be
“OLYMPUS” Single Use Guide Sheath Kit
TW: “奧林柏斯”單次使用導引套管組
Taiwan·Risk Class 2·MD·AOMORI OLYMPUS CO., LTD.·Registered Apr 19, 2020 – Apr 19, 2025ExpiredRegistration details
- Analysis ID
- 913b792d874769ec32dee07fbe3979be
- License Form
- Ministry of Health Medical Device Import No. 033443
- Customs Code
- DHA05603344307
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
- Apr 19, 2020
- Expiry Date
- Apr 19, 2025
About this record
Access comprehensive regulatory information for “OLYMPUS” Single Use Guide Sheath Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 913b792d874769ec32dee07fbe3979be and manufactured by AOMORI OLYMPUS CO., LTD.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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