Taiwan FDA registration 6084e5802f51ee48a2d6d7c56c561594
“OLYMPUS” EVIS LUCERA ELITE DUODENOVIDEOSCOPE
TW: “奧林柏斯”處置型十二指腸鏡
Taiwan·Risk Class 2·MD·AIZU OLYMPUS CO., LTD·Registered Oct 28, 2021 – Oct 28, 2026ActiveRegistration details
- Analysis ID
- 6084e5802f51ee48a2d6d7c56c561594
- License Form
- Ministry of Health Medical Device Import No. 034989
- Customs Code
- DHA05603498904
Company information
- Manufacturer
- AIZU OLYMPUS CO., LTD
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Oct 28, 2021
- Expiry Date
- Oct 28, 2026
About this record
Access comprehensive regulatory information for “OLYMPUS” EVIS LUCERA ELITE DUODENOVIDEOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6084e5802f51ee48a2d6d7c56c561594 and manufactured by AIZU OLYMPUS CO., LTD. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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