Taiwan FDA registration cb0b260833a57d3a15868a52c124a5cc
“OLYMPUS” VISERA 4K UHD Xenon Light Source and Accessories
TW: “奧林柏斯”光源裝置及其附件
Registration details
- Analysis ID
- cb0b260833a57d3a15868a52c124a5cc
- License Form
- Ministry of Health Medical Device Import No. 028732
- Customs Code
- DHA05602873207
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
- Aug 15, 2016
- Expiry Date
- Aug 15, 2026
About this record
Access comprehensive regulatory information for “OLYMPUS” VISERA 4K UHD Xenon Light Source 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 cb0b260833a57d3a15868a52c124a5cc and manufactured by SHIRAKAWA 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