Taiwan FDA registration 117ffd28bc9acc68c15501203ea19275
“OLYMPUS” ENDOEYE FLEX Deflectable Videoscope and Accessories
TW: “奧林柏斯”電子式腹腔鏡及其附件
Taiwan·Risk Class 2·MD·AIZU OLYMPUS CO., LTD.·Registered Aug 25, 2014 – Aug 25, 2024ExpiredRegistration details
- Analysis ID
- 117ffd28bc9acc68c15501203ea19275
- License Form
- Ministry of Health Medical Device Import No. 026483
- Customs Code
- DHA05602648302
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
- Aug 25, 2014
- Expiry Date
- Aug 25, 2024
About this record
Access comprehensive regulatory information for “OLYMPUS” ENDOEYE FLEX Deflectable Videoscope and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 117ffd28bc9acc68c15501203ea19275 and manufactured by AIZU OLYMPUS CO., LTD.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices